Ink jet liquid composition and ink jet recording method

ABSTRACT

An ink jet liquid composition contains an organic solvent, a polymerizable compound, a photopolymerization initiator, and a polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, and the content of the organic solvent is 40% by mass or more and 90% by mass or less with respect to the total mass of the composition. In addition, an ink jet recording method using the ink jet liquid composition is provided.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of International Application No. PCT/JP2018/004069, filed Feb. 6, 2018, the disclosure of which is incorporated herein by reference in its entirety. Further, this application claims priority from Japanese Patent Application No. 2017-037215, filed Feb. 28, 2017, the disclosure of which is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION 1. Field of the Invention

The present disclosure relates to an ink jet liquid composition and an ink jet recording method.

2. Description of the Related Art

As an image recording method of forming an image on a recording medium such as paper or plastic, based on an image data signal, there are an electrophotographic method, a sublimation-type or fusion-type thermal transfer method, a screen printing method, and an ink jet method.

In the ink jet method, a printing device is inexpensive, a plate is not required at the time of printing, and image formation is directly carried out on a recording medium by jetting an ink composition only to a necessary image area. Thus, the ink composition can be used with excellent efficiency, and the running cost becomes low particularly in a case of small lot production. Further, the ink jet method generates little noise and is excellent as an image recording method. Therefore, the ink jet method has been attracting attention in recent years.

In addition, as an ink jet ink, a solvent ink, an aqueous ink, an ultraviolet curable-type ink, an ultraviolet curable-type solvent ink (solvent UV ink), and the like may be exemplified.

Conventional ink jet ink compositions include compounds described in JP2006-181801A, JP2016-020457A, JP2013-163740A, or JP2016-000819A.

SUMMARY OF THE INVENTION

An object of an embodiment of the present invention is to provide an ink jet liquid composition with which even in a case of forming a cured film using a base material having a concave-convex shape, the obtained cured film has excellent abrasion resistance and excellent chemical resistance.

Another object of another embodiment of the present invention to provide an ink jet recording method using the ink jet liquid composition.

Means for achieving the above objects includes the following aspects.

<1> An ink jet liquid composition comprising: an organic solvent; a polymerizable compound; a photopolymerization initiator; and a polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, in which a content of the organic solvent is 40% by mass or more and 90% by mass or less with respect to a total mass of the composition.

<2> The ink jet liquid composition according to <1>, in which a content of a siloxane structure of the polyether-modified siloxane compound is 20% by mass or more with respect to a total mass of the polyether-modified siloxane compound.

<3> The ink jet liquid composition according to <1> or <2>, in which the polyether-modified siloxane compound has a weight-average molecular weight of 5,000 or more and 100,000 or less.

<4> The ink jet liquid composition according to any one of <1> to <3>, in which a content of the polyether-modified siloxane compound is 2% by mass or more and 15% by mass or less with respect to a total solid content of the composition.

<5> The ink jet liquid composition according to any one of <1> to <4>, in which a mass ratio of the polyether-modified siloxane compound and the polymerizable compound is polyether-modified siloxane compound:polymerizable compound=1:5 to 1:30.

<6> The ink jet liquid composition according to any one of <1> to <5>, in which the polymerizable compound includes a bifunctional urethane acrylate oligomer.

<7> The ink jet liquid composition according to <6>, in which the bifunctional urethane acrylate oligomer has a weight-average molecular weight of 3,000 or more and 20,000 or less.

<8> The ink jet liquid composition according to any one of <1> to <7>, in which a colorant is not contained.

<9> The ink jet liquid composition according to any one of <1> to <8> that is an ink jet liquid composition to be applied to a base material having a concave-convex shape in at least a part of a surface.

<10> An ink jet recording method comprising: a step of applying the ink jet liquid composition according to any one of <1> to <9> to a base material by an ink jet recording head.

<11> The ink jet recording method according to <10>, in which the base material is a base material having a concave-convex shape in at least a part of a surface.

<12> An ink jet recording method comprising: a step of preparing a base material having a decorative layer formed thereon; a step of applying the ink jet liquid composition according to <8> to the decorative layer by an ink jet recording head; a step of drying the ink jet liquid composition on the decorative layer by applying heat; and a step of curing the ink jet liquid composition by irradiating the ink jet liquid composition with an ultraviolet ray, in which the base material having the decorative layer formed thereon has a concave-convex shape in at least a part of a surface.

According to an embodiment of the present invention, it is possible to provide an ink jet liquid composition with which even in a case of forming a cured film using a base material having a concave-convex shape, the obtained cured film has excellent abrasion resistance and excellent chemical resistance.

According to another embodiment of the present invention, it is possible to provide an ink jet recording method using the ink jet liquid composition.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Hereinafter, the present disclosure will be described in detail.

In present specification, “xx to yy” refers to a numerical value range that includes xx and yy.

In present specification, the term “(meta)acrylic” is a term used as a concept encompassing both acrylic and methacrylic, and the term “(meth)acryloyl” is a term used as a concept encompassing both acryloyl and methacryloyl.

A hydrocarbon group such as an alkyl group, an aryl group, an alkylene group or an arylene group in the present disclosure may have a branch or a ring structure unless otherwise specified.

In addition, in the present disclosure, “% by mass” and “% by weight” are the same and “parts by mass” and “parts by weight” are the same.

In addition, the term “step” in the present specification means not only an independent step but also a step in which an expected object in the step is attained even in a case where the step cannot be clearly distinguished from other steps. In addition, in the present disclosure, a combination of two or more preferable embodiments is a more preferable embodiment.

Further, the weight-average molecular weight (Mw) in the present disclosure is a molecular weight detected by using a gel permeation chromatography (GPC) analyzer using columns of TSKgel GMHxL, TSKgel G4000HxL, and TSKgel G2000HxL (all trade name, manufactured by Tosoh Corporation), tetrahydrofuran (THF) as a solvent, and a differential refractometer and shown in terms of polystyrene as a standard substance, unless otherwise specified.

Hereinafter, the present disclosure will be described in detail.

(Ink Jet Liquid Composition)

An ink jet liquid composition according to an embodiment of the present disclosure (hereinafter, also simply referred to as a “liquid composition”) contains an organic solvent, a polymerizable compound, a photopolymerization initiator, and a polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, and a content of the organic solvent is 40% by mass or more and 90% by mass or less with respect to the total mass of the composition.

As a result of detailed examinations conducted by the present inventors, it has been found that by adopting an ink jet liquid composition having the above composition, even in a case where a cured film is formed using a base material having a concave-convex shape, the obtained cured film has excellent abrasion resistance and excellent chemical resistance.

Although the detailed mechanism is unknown, it is assumed that by setting the content of the organic solvent to 40% by mass or more and 90% by mass or less with respect to the total mass of the liquid composition, a dried film with a thin film thickness in which components other than the organic solvent are uniformly applied is easily formed and cured to obtain a tough cured film so that the obtained cured film has excellent abrasion resistance and excellent chemical resistance.

In addition, by containing the polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, the viscosity increase in the composition at the time of drying is fast, even in a case where a base material having a concave-convex shape is used, followability to the concave-convex shape is excellent, a composition reservoir is prevented from being formed in the concave portion, and a cured film is prevented from not being formed or a thin portion is prevented from being formed in the convex portion, and further, a tough cured film is obtained. Thus, it is assumed that the obtained cured film has excellent abrasion resistance and excellent chemical resistance.

Hereinafter, the present disclosure will be described in detail.

The ink jet liquid composition according to the embodiment of the present disclosure can be suitably used as an ink jet liquid composition to be applied to a base material having a concave-convex shape in at least a part of the surface such as leather and can be more suitably used as an ink jet liquid composition to be applied to leather.

Regarding the term “to be applied to the base material”, the liquid composition may be directly applied to the base material or after a layer such as a decorative layer is provided to the base material, the liquid composition may be applied to the layer.

The leather is not particularly limited, and examples thereof include natural leather, synthetic leather, and artificial leather. In addition, the above-mentioned leather may be one subjected to treatment such as tanning.

It is needless to say that the ink jet liquid composition according to the embodiment of the present disclosure may be applied to a base material having a concave-convex shape in at least a part of the surface and a normal smooth base material.

The term “concave-convex shape” of the surface of the base material or the surface of the base material on which a decorative layer, which will be described later, is formed thereon in the present disclosure is a portion satisfying Expression R. L2≥1.05×L1  Expression R

For L1 and L2, the following lengths are measured on the base material by a confocal laser microscope.

L1: a projection length between a point A on the surface of the base material where the cross-sectional shape is analyzed by a confocal laser microscope and a point B on the same base material surface as the point A (projection distance between point A and point B)

L2: a length from the point A calculated from the cross-sectional shape measured by a confocal laser microscope to the point B along the concave-convex shape on the base material surface (length of cross-sectional curve between point A and point B)

In a normal smooth base material, the value of L2 is less than 1.05 times the value of L1.

As the confocal laser microscope, a shape analysis laser microscope (VK-X 250/260) manufactured by Keyence Corporation may be suitably used.

In addition, from the viewpoint of further exerting the effects of the liquid composition according to the embodiment of the present disclosure, the base material used in the present disclosure is preferably a base material having a portion satisfying Expression R-1 in at least a part of the surface, more preferably a base material having a portion satisfying Expression R-2 in at least a part of the surface, and even more preferably a base material having a portion satisfying Expression R-3 in at least a part of the surface. L2≥1.10×L1  Expression R-1 5×L1≥L2≥1.10×L1  Expression R-2 3×L1≥L2≥1.20×L1  Expression R-3

The base material used in the present disclosure is preferably a base material having a concave-convex shape in an area of 50% by area or more of the surface on at least one surface, and more preferably a base material having a concave-convex shape in an area of 70% by area or more of the surface on at least one surface.

The liquid composition according to the embodiment of the present disclosure is an ink composition that is curable by active radiation. The term “active radiation” refers to a radiation capable of imparting energy to generate an initiating species in the liquid composition by the irradiation and includes an α-ray, a γ-ray, an X-ray, an ultraviolet ray, a visible ray, an electron beam and the like. Among these, from the viewpoint of curing sensitivity and easy availability of the apparatus, an ultraviolet ray, and an electron beam are preferable and an ultraviolet ray is more preferable.

The liquid composition according to the embodiment of the present disclosure preferably contains as little water as possible and even in a case where the liquid composition contains water, the water content is preferably 5% by mass or less, more preferably 1% by mass or less, and even more preferably 0.5% by mass or less with respect to the total mass of the liquid composition.

In addition, the liquid composition according to the embodiment of the present disclosure can be used for various applications such as an ink composition, a resist, an image recording layer of a planographic printing plate precursor, a coating agent, a paint, an adhesive, a pressure sensitive adhesive, a coating composition, a functional film, a film, an optical material, a printing plate material, a semiconductor material, a recording material, a paper additive, a medical material, a plastic, a functional gel, and a cosmetic material. Among these, the liquid composition can be suitably used for a coating composition or an ink composition and more suitably used for a coating composition.

Further, the liquid composition can be more suitably used for a coating composition for protecting the decorative layer on the base material, and particularly suitably used for a coating composition for protecting a decorative layer on leather.

Hereinafter, each component used in the liquid composition according to the embodiment of the present disclosure will be described in detail.

<Organic Solvent>

The ink jet liquid composition according to the embodiment of the present disclosure contains an organic solvent, and the content of the organic solvent is 40% by mass or more and 90% by mass or less with respect to the total mass of the liquid composition.

As the organic solvent, known solvents used for solvent inks and active radiation curable solvent inks can be used, and examples thereof include organic solvents described in New Edition Solvent Pocketbook (The Society of Synthetic Organic Chemistry, Japan, 1994).

In addition, the organic solvent is preferably an organic solvent having a boiling point of 150° C. or higher and 250° C. or lower and more preferably an organic solvent having a boiling point of 150° C. or higher and 200° C. or lower from the viewpoint of ink jet jettability, and the abrasion resistance and chemical resistance of the obtained cured film.

The organic solvents that can be used in the present disclosure may be used singly or in combination of two or more thereof.

Examples of the organic solvent include (poly)alkylene glycol monoalkyl ethers such as diethylene glycol monoethyl ether, triethylene glycol monomethyl ether, dipropylene glycol monomethyl ether, and tripropylene glycol monomethyl ether, (poly)alkylene glycol dialkyl ethers such as ethylene glycol dibutyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, dipropylene glycol diethyl ether, and tetraethylene glycol dimethyl ether, (poly)alkylene glycol acetates such as diethylene glycol acetate, (poly)alkylene glycol diacetates such as ethylene glycol diacetate and propylene glycol diacetate, (poly)alkylene glycol monoalkyl ether acetates such as ethylene glycol monobutyl ether acetate and propylene glycol monomethyl ether acetate, ketones such as methyl ethyl ketone and cyclohexanone, lactones such as γ-butyrolactone, esters such as ethyl acetate, propyl acetate, butyl acetate, 3-methoxybutyl acetate, methyl propionate, and ethyl propionate, cyclic ethers such as tetrahydrofuran and dioxane, and amides such as dimethylformamide and dimethylacetamide.

In addition, as the (poly)alkylene glycol is preferably at least one compound selected from the group consisting of (poly)ethylene glycol and (poly)propylene glycol.

Among these, from the viewpoint of ink jet jettability, and the chemical resistance of the obtained cured film, it is preferable to use at least one organic solvent selected from the group consisting of alkylene glycol monoalkyl ether acetates, alkylene glycol monoalkyl ethers, alkylene glycol dialkyl ethers, alkylene glycol acetates, polyalkylene glycol monoalkyl ether acetates, polyalkylene glycol monoalkyl ethers, polyalkylene glycol dialkyl ethers, polyalkylene glycol acetates, ketones, lactones, and esters, it is more preferable to use at least one organic solvent selected from the group consisting of alkylene glycol monoalkyl ether acetates, alkylene glycol dialkyl ethers, polyalkylene glycol monoalkyl ether acetates, polyalkylene glycol dialkyl ethers, ketones, lactones, and esters, it is even more preferable to use esters, and it is particularly preferable to use 3-methoxybutyl acetate.

The content of the organic solvent in the ink jet liquid composition according to the embodiment of the present disclosure is 40% by mass or more and 90% by mass or less with respect to the total mass of the liquid composition, and is preferably 50% by mass or more and 88% by mass or less, more preferably 65% by mass or more and 86% by mass or less, and particularly preferably 75% by mass or more and 84% by mass or less from the viewpoint of ink jet jettability and the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

<Polyether-Modified Siloxane Compound Having Weight-Average Molecular Weight of 3,000 or More>

The ink jet liquid composition according to the embodiment of the present disclosure contains a polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more.

The polyether-modified siloxane compound in the present disclosure is not particularly limited as long as the polyether-modified siloxane compound is a compound having a polyether structure and a siloxane structure. However, from the viewpoint of ink jet jettability, and the abrasion resistance, chemical resistance, and adhesiveness of the obtained cured film, the content of a siloxane structure of a polyether-modified siloxane compound is preferably 15% by mass or more, more preferably 20% by mass or more, even more preferably 20% by mass or more and 90% by mass or less, and particularly preferably 20% by mass or more and 50% by mass or less with respect to the total mass of the polyether-modified siloxane compound.

In the present disclosure, the content of the siloxane structure of the polyether-modified siloxane compound can be quantitatively determined by various nuclear magnetic resonance (NMR) analysis and MALDI-MS analysis (mass spectrometry using matrix-assisted laser desorption ionization).

The siloxane structure may be a —(SiR^(S1)R^(S2)—O)_(n)— structure (R^(S1) and R^(S2) each independently represent a hydrogen atom, a hydroxy group, an alkoxy group, an alkyl group or an aryl group, and n represents an integer of 1 or more), and is preferably at least one structure selected from the group consisting of a polydialkylsiloxane structure and a polyalkylaryl siloxane structure, more preferably a polydialkylsiloxane structure, and particularly preferably a polydimethylsiloxane structure.

As the polyether structure, a polyalkyleneoxy structure is preferably exemplified, and at least one structure selected from the group consisting of a polyethyleneoxy structure and a polypropyleneoxy structure is more preferably exemplified.

The weight-average molecular weight of the polyether-modified siloxane compound used in the ink jet liquid composition according to the present disclosure is 3,000 or more, from the viewpoint of ink jet jettability, and the bendability and adhesiveness of the obtained cured film, is preferably 5,000 or more, more preferably 5,000 or more and 100,000 or less, even more preferably 8,000 or more and 50,000 or less, and particularly preferably 10,000 or more and 20,000 or less.

As the polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, a commercially available product may be used. Examples of commercially available products include KP109, KP368, KP306, KP341, KF-96H-10,000 CS, KF-96H-30,000 CS, and KF-96H-100,000 CS (all manufactured by Shin-Etsu Chemical Co., Ltd.), and BYK-UV3500 (manufactured by BYK Chemie GmbH).

These polyether-modified siloxane compounds may be used singly or in combination of two or more thereof.

The content of the polyether-modified siloxane compound in the ink jet liquid composition according to the present disclosure is preferably 1% by mass or more and 20% by mass or less, more preferably 2% by mass or more and 15% by mass or less, and particularly preferably 2.5% by mass or more and 10% by mass or less with respect to the total solid content of the composition from the viewpoint of ink jet jettability, and the abrasion resistance, chemical resistance, and adhesiveness of the obtained cured film. The “solid content” in the composition represents a component excluding volatile components such as an organic solvent.

In addition, in the ink jet liquid composition according to the present disclosure, the mass ratio of the polyether-modified siloxane compound and the polymerizable compound is preferably polyether-modified siloxane compound:polymerizable compound=1:3 to 1:50 and more preferably 1:5 to 1:30 from the viewpoint of ink jet jettability, and the abrasion resistance, chemical resistance, and adhesiveness of the obtained cured film.

Further, in the ink jet liquid composition according to the present disclosure, the mass ratio of the polyether-modified siloxane compound and a vinyl chloride-vinyl acetate copolymer described later is preferably polyether-modified siloxane compound:vinyl chloride-vinyl acetate copolymer=10:1 to 1:1, more preferably 5:1 to 1:1, and even more preferably 5:1 to 2:1 from the viewpoint of the abrasion resistance, chemical resistance, and adhesiveness of the obtained cured film.

<Polymerizable Compound>

The ink jet liquid composition according to the present disclosure includes a polymerizable compound.

The polymerizable compound is not particularly limited as long as the compound is a compound that causes a polymerization reaction upon application of any energy to be cured, and any kind of monomer, oligomer or polymer can be used. In particular, various known polymerizable monomers known as radical polymerizable monomers, which cause a polymerization reaction by initiating species generated from a polymerization initiator added as requested, are preferable.

In addition, the polymerizable compound is preferably an ethylenically unsaturated compound.

Further, the polymerizable compound in the present disclosure is a compound other than the polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, and is preferably a compound which does not have both a polyether structure and a siloxane structure.

The polymerizable compound can be used as a mixture of one or more for the purpose of adjusting the reaction rate, the physical properties of the cured film, the physical properties of the composition, and the like. In addition, the polymerizable compound may be a monofunctional compound or a polyfunctional compound. In a case where the ratio of the monofunctional polymerizable compound is large, the cured product easily becomes flexible, and in a case where the ratio of the polyfunctional polymerizable compound is large, the curability easily becomes excellent. Accordingly, the ratio between the monofunctional polymerizable compound and the polyfunctional polymerizable compound is arbitrarily determined according to the application.

The polymerizable compound used in the present disclosure preferably contains a urethane (meth)acrylate oligomer from the viewpoints of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

The urethane (meth)acrylate oligomer in the present disclosure may be a compound having one or more urethane bonds and having a (meth)acryloxy group.

It is preferable that the ink jet liquid composition according to the embodiment of the present disclosure includes a bifunctional urethane (meth)acrylate oligomer from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film, and it is more preferable that the weight-average molecular weight of the bifunctional urethane (meth)acrylate oligomer is 3,000 or more and 20,000 or less from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

Also, in the present disclosure, the oligomer has a weight-average molecular weight of 500 or more and 20,000 or less, and the polymer has a weight-average molecular weight of more than 20,000.

As the bifunctional urethane (meth)acrylate oligomer, a commercially available product may be used.

Examples of the commercially available product include CN9001 (manufactured by Sartomer Company Inc.), and SHIKO UV-3200B, SHIKO UV-3300B, SHIKO UV-3310B, and SHIKO UV-6630B (all manufactured by The Nippon Synthetic Chemical Industry Co., Ltd.).

In addition, the polymerizable compound used in the present disclosure preferably includes a trifunctional or higher functional urethane (meth)acrylate oligomer and more preferably includes a bifunctional urethane (meth)acrylate oligomer and a trifunctional or higher urethane (meth)acrylate oligomer from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

The functional number of the trifunctional or higher urethane (meth)acrylate oligomer is preferably 3 or more and 12 or less, and more preferably 3 or more and 6 or less from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

In a case where as the polymerizable compound, a bifunctional urethane (meth)acrylate oligomer and a trifunctional or higher urethane (meth)acrylate oligomer are used in combination, the content ratio (mass ratio) of the bifunctional urethane (meth)acrylate oligomer and the trifunctional or higher urethane (meth)acrylate oligomer in the ink jet liquid composition according to the embodiment of the present disclosure is preferably bifunctional urethane (meth)acrylate oligomer:trifunctional or higher urethane (meth)acrylate oligomer=3:1 to 1:2, more preferably 2:1 to 1:1.5, and even more preferably 1.5:1 to 1:1.5 from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

As the trifunctional or higher urethane (meth)acrylate oligomer, a commercially available product may be used.

Examples of commercially available products include SHIKO UV-7600B and SHIKO UV-7550B (all manufactured by Nippon Synthetic Chemical Industry Co., Ltd.).

The weight-average molecular weight (Mw) of the urethane (meth)acrylate oligomer is preferably 500 or more and 20,000 or less, more preferably 1,000 or more and 10,000 or less, and even more preferably 1,200 or more and 6,000 or less from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

The content of the urethane (meth)acrylate oligomer in the ink jet liquid composition according to the embodiment of the present disclosure is preferably 1% by mass or more and 50% by mass or less, more preferably 3% by mass or more and 30% by mass or less, and particularly preferably 5% by mass or more and 20% by mass or less with respect to the total mass of the composition from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

In addition, the content of the bifunctional urethane (meth)acrylate oligomer in the ink jet liquid composition according to the embodiment of the present disclosure is preferably 0.5% by mass or more and 50% by mass or less, more preferably 1% by mass or more and 20% by mass or less, and particularly preferably 2% by mass or more and 10% by mass or less with respect to the total mass of the composition from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

In addition, the content of the trifunctional or higher urethane (meth)acrylate oligomer in the ink jet liquid composition according to the embodiment of the present disclosure is preferably 0.5% by mass or more and 20% by mass or less, more preferably 1% by mass or more and 15% by mass or less, and particularly preferably 2% by mass or more and 10% by mass or less with respect to the total mass of the composition from the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film.

In addition, examples of the polymerizable compound include (meth)acrylate compounds, (meth)acrylamide compounds, and aromatic vinyl compounds.

Examples of (meth)acrylate compounds used as the polymerizable compound include monofunctional (meth)acrylate compounds, bifunctional (meth)acrylate compounds, trifunctional (meth)acrylate compounds, tetrafunctional (meth)acrylate compounds, pentafunctional (meth)acrylate compounds, and hexafunctional (meth)acrylate compounds.

Examples of the monofunctional (meth)acrylate compounds include hexyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, tert-octyl (meth)acrylate, isoamyl (meth)acrylate, decyl (meth)acrylate, isodecyl (meth)acrylate, stearyl (meth)acrylate, isostearyl (meth)acrylate, cyclohexyl (meth)acrylate, 4-n-butylcyclohexyl (meth)acrylate, bornyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, 2-ethylhexyldiglycol (meth)acrylate, butoxyethyl (meth)acrylate, 2-chloroethyl (meth)acrylate, 4-bromobutyl (meth)acrylate, cyanoethyl (meth)acrylate, benzyl (meth)acrylate, butoxymethyl (meth)acrylate, 3-methoxybutyl (meth)acrylate, 2-(2-methoxyethoxy)ethyl (meth)acrylate, 2-(2-butoxyethoxy)ethyl (meth)acrylate, 2,2,2-tetrafluoroethyl (meth)acrylate, 1H,1H,2H,2H-perfluorodecyl (meth)acrylate, 4-butylphenyl (meth)acrylate, phenyl (meth)acrylate, 2,4,5-tetramethylphenyl (meth)acrylate, 4-chlorophenyl (meth)acrylate, phenoxymethyl (meth)acrylate, phenoxyethyl (meth)acrylate, glycidyl (meth)acrylate, glycidyloxybutyl (meth)acrylate, glycidyloxyethyl (meth)acrylate, glycidyloxypropyl (meth)acrylate, tetrahydrofurfuryl (meth)acrylate, 2-hydroxyethyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate.

4-hydroxybutyl (meth)acrylate, 3-hydroxybutyl (meth)acrylate, dimethylaminoethyl (meth)acrylate, diethylaminoethyl (meth)acrylate, dimethylaminopropyl (meth)acrylate, diethylaminopropyl (meth)acrylate, trimethoxysilylpropyl (meth)acrylate, trimethylsilylpropyl (meth)acrylate, polyethylene oxide monomethyl ether (meth)acrylate, oligoethylene oxide monomethyl ether (meth)acrylate, polyethylene oxide (meth)acrylate, oligoethylene oxide (meth)acrylate, oligoethylene oxide monoalkyl ether (meth)acrylate, polyethylene oxide monoalkyl ether (meth)acrylate, dipropylene glycol (meth)acrylate, polypropylene oxide monoalkyl ether (meth)acrylate, oligopropylene oxide monoalkyl ether (meth)acrylate, 2-methacryloyloxyethylsuccinic acid, 2-methacryloyloxyhexahydrophthalic acid, 2-methacryloyloxyethyl-2-hydroxypropyl phthalate, butoxydiethylene glycol (meth)acrylate, trifluoroethyl (meth)acrylate, perfluorooctylethyl (meth)acrylate, 2-hydroxy-3-phenoxypropyl (meth)acrylate, ethylene oxide (EO)-modified phenol (meth)acrylate, EO-modified cresol (meth)acrylate, EO-modified nonyl phenol (meth)acrylate, propylene oxide (PO)-modified nonyl phenol (meth)acrylate, EO-modified 2-ethylhexyl (meth)acrylate, dicyclopentenyl (meth)acrylate, dicyclopentenyl oxy ethyl (meth)acrylate, an dicyclopentanyl (meth)acrylate, (3-ethyl-3-oxetanyl methyl) (meth)acrylate, and phenoxyethylene glycol (meth)acrylate.

Examples of bifunctional (meth)acrylate compounds include 1,6-hexanediol di(meth)acrylate, 1,10-decanediol di(meth)acrylate, neopentyl glycol di(meth)acrylate, 2,4-dimethyl-1,5-pentanediol di(meth)acrylate, 3-methyl-1,5-pentanediol di(meth)acrylate, butylethylpropanediol di(meth)acrylate, ethoxylated cyclohexane methanol di(meth)acrylate, polyethylene glycol di(meth)acrylate, oligoethylene glycol di(meth)acrylate, ethylene glycol di(meth)acrylate, 2-ethyl-2-butyl-butanediol di(meth)acrylate, hydroxypivalic acid neopentyl glycol di(meth)acrylate, EO-modified bisphenol A di(meth)acrylate, bisphenol F polyethoxy di(meth)acrylate, polypropylene glycol di(meth)acrylate, oligopropylene glycol di(meth)acrylate, 1,4-butanediol di(meth)acrylate, 2-ethyl-2-butylpropanediol di(meth)acrylate, 1,9-nonane di(meth)acrylate, propoxylated ethoxylated bisphenol A di(meth)acrylate, tricyclodecane di(meth)acrylate, dipropylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, and PO-modified neopentyl glycol di(meth)acrylate.

Examples of trifunctional (meth)acrylate compounds include trimethylolpropane tri(meth)acrylate, trimethylolethane tri(meth)acrylate, trimethylolpropane alkylene oxide-modified tri(meth)acrylate, pentaerythritol tri(meth)acrylate, dipentaerythritol tri(meth)acrylate, trimethylolpropane tri((meth)acryloyloxypropyl)ether, isocyanuric acid alkylene oxide-modified tri(meth)acrylate, propionic acid dipentaerythritol tri(meth)acrylate, tri((meth)acryloyloxyethyl) isocyanurate, hydroxypival aldehyde-modified dimethylolpropane tri(meth)acrylate, sorbitol tri(meth)acrylate, propoxylated trimethylolpropane tri(meth)acrylate, and ethoxylated glycerin triacrylate.

Examples of tetrafunctional (meth)acrylate compounds include pentaerythritol tetra(meth)acrylate, sorbitol tetra(meth)acrylate, ditrimethylolpropane tetra(meth)acrylate, propionic acid dipentaerythritol tetra(meth)acrylate, and ethoxylated pentaerythritol tetra(meth)acrylate.

Examples of pentafunctional (meth)acrylate compounds include sorbitol penta(meth)acrylate and dipentaerythritol penta(meth)acrylate.

Examples of hexafunctional (meth)acrylate compounds include dipentaerythritol hexa(meth)acrylate, sorbitol hexa(meth)acrylate, phosphazene alkylene oxide-modified hexa(meth)acrylate, and ε-caprolactone-modified dipentaerythritol hexa(meth)acrylate.

Examples of (meth)acrylamide compounds used as the radical polymerizable compound include (meth)acrylamide, N-methyl (meth)acrylamide, N-ethyl (meth)acrylamide, N-propyl (meth)acrylamide, N-n-butyl (meth)acrylamide, N-t-butyl (meth)acrylamide, N-butoxymethyl (meth)acrylamide, N-isopropyl (meth)acrylamide, N-methylol (meth)acrylamide, N,N-dimethyl (meth)acrylamide, N,N-diethyl (meth)acrylamide, and (meth)acryloyl morpholine.

Examples of aromatic vinyls used as the radical polymerizable compound include styrene, dimethyl styrene, trimethyl styrene, isopropyl styrene, chloromethyl styrene, methoxy styrene, acetoxy styrene, chlorostyrene, dichlorostyrene, bromostyrene, methyl ester vinylbenzoate, 3-methyl styrene, 4-methyl styrene, 3-ethyl styrene, 4-ethyl styrene, 3-propyl styrene, 4-propyl styrene, 3-butyl styrene, 4-butyl styrene, 3-hexyl styrene, 4-hexyl styrene, 3-octyl styrene, 4-octyl styrene, 3-(2-ethylhexyl) styrene, 4-(2-ethylhexyl) styrene, allyl styrene, isopropenyl styrene, butenyl styrene, octenyl styrene, 4-t-butoxycarbonyl styrene, and 4-t-butoxy styrene.

Further, examples of the radical polymerizable compound in the present disclosure include vinyl ester compounds (such as vinyl acetate, vinyl propionate, and vinyl versate), allyl ester compounds (such as allyl acetate), halogen-containing monomers (such as vinylidene chloride, and vinyl chloride), vinyl ethers (such as methyl vinyl ether, butyl vinyl ether, hexyl vinyl ether, methoxy vinyl ether, 2-ethyl hexyl vinyl ether, methoxyethyl vinyl ether, cyclohexyl vinyl ether, chloroethyl vinyl ether, and triethyleneglycol divinyl ether), vinyl cyanides (such as (meth)acrylonitrile), and olefin compounds (such as ethylene, and propylene), and N-vinyl lactam compounds (such as N-vinylcaprolactam).

More specifically, commercially available products or radically polymerizable or crosslinking monomers, oligomers, and polymers that are industrially known, such as those described in “Crosslinking Agent Handbook” edited by Shinzo Yamashita (1981, Taiseisha Ltd.); “UV⋅EB Curing Handbook (raw material edition)” edited by Kiyoshi Kato (1985, Koubunshi Kankoukai); “Application and Market of UV⋅EB Curing Technique”, p. 79, edited by RadTech Japan (1989, CMC Publishing Co., Ltd.); “Polyester Resin Handbook” edited by Eiichiro Takiyama (1988, The Nikkan Kogyo Shimbun, Ltd.) and the like can be used.

These polymerizable compounds may be used singly or in combination of two or more thereof.

The content of the polymerizable compound in the ink jet liquid composition according to the embodiment of the present disclosure is also related to the application, but is preferably 10% by mass to 95% by mass and more preferably 20% by mass to 90% by mass with respect to the total solid content of the composition from the viewpoint of curability.

From the viewpoint of the abrasion resistance, bendability, and chemical resistance of the obtained cured film, the content of polymerizable compounds other than the urethane (meth)acrylate oligomer in the ink jet liquid composition according to the embodiment of the present disclosure is preferably 50% by mass or less, more preferably 20% by mass or less, and even more preferably 5% by mass or less with respect to the total solid content of the composition and other polymerizable compounds are particularly preferably not included in the composition.

<Photopolymerization Initiator>

The ink jet liquid composition according to the embodiment of the present disclosure contains a photopolymerization initiator.

As the photopolymerization initiator that can be used in the present disclosure, a photoradical polymerization initiator is preferably used from the viewpoint of excellent curability and fixing property.

The photopolymerization initiator in the present disclosure is a compound that causes a chemical change through the action of light or interaction with the electron excited state of a sensitizer to generate a polymerization initiating species, and among these compounds, from the viewpoint of initiating polymerization by simple means of exposure, a photopolymerization initiator is preferable.

The photopolymerization initiator can be selected from photopolymerization initiators sensitive to active radiation to be emitted such as an ultraviolet ray in a range of 400 nm to 200 nm, a far ultraviolet ray, a g-ray, an h-ray, an i-ray, a KrF excimer laser beam, an ArF excimer laser beam, an electron beam, an X-ray, a molecular beam or an ion beam.

Preferable examples of the photopolymerization initiator includes (a) aromatic ketones, (b) aromatic onium salts, (c) organic peroxides, (d) hexaarylbiimidazole compounds, (e) ketoxime ester compounds, (f) borate compounds, (g) azinium compounds, (h) metallocene compounds, (i) active ester compounds, and (j) carbon-halogen bond-containing compounds.

As the photoradical polymerization initiator, from the viewpoint of curability, aromatic ketones are preferable.

In addition, as the photoradical polymerization initiator, an acylphosphine oxide compound is preferable.

As the acylphosphine oxide compound, a monoacylphosphine oxide compound, a bisacylphosphine oxide compound, and the like can be used, and as the monoacylphosphine oxide compound, a known monoacylphosphine oxide compound can be used. Examples thereof include monoacylphosphine oxide compounds described in JP1985-008047B (JP-S60-008047B) and JP1988-040799B (JP-S63-040799B). Specific examples thereof include methyl isobutyrylmethylphosphinate, methyl isobutyrylphenylphosphinate, methyl pivaloylphenylphosphinate, methyl 2-ethylhexanoylphenylphosphinate, isopropyl pivaloylphenylphosphinate, methyl p-toluylphenylphosphinate, methyl o-toluylphenylphosphinate, methyl 2,4-dimethylbenzoylphenylphosphinate, isopropyl p-t-butylbenzoylphenylphosphinate, methyl acryloylphenylphosphinate, isobutyryldiphenylphosphine oxide, 2-ethylhexanoyldiphenylphosphine oxide, o-toluyldiphenylphosphine oxide, p-t-butylbenzoyldiphenylphosphine oxide, 3-pyridylcarbonyldiphenylphosphine oxide, acryloyldiphenylphosphine oxide, benzoyldiphenylphosphine oxide, vinyl pivaloylphenylphosphinate, adipoylbisdiphenylphosphine oxide, pivaloyldiphenylphosphine oxide, p-toluyldiphenylphosphine oxide, 4-(t-butyl)benzoyldiphenylphosphine oxide, 2-methylbenzoyldiphenylphosphine oxide, 2-methyl-2-ethylhexanoyldiphenylphosphine oxide, 1-methylcyclohexanoyldiphenylphosphine oxide, methyl pivaloylphenylphosphinate, and isopropyl pivaloylphenylphosphinate.

As the bisacylphosphine oxide compound, a known bisacylphosphine oxide compound may be used. Examples thereof include bisacylphosphine oxide compounds described in JP1991-101686A (JP-H03-101686A), JP1993-345790A (JP-H05-345790A), and JP1994-298818A (JP-H06-298818A). Specific examples thereof include bis(2,6-dichlorobenzoyl)phenylphosphine oxide, bis(2,6-dichlorobenzoyl)-2,5-dimethylphenylphosphine oxide, bis(2,6-dichlorobenzoyl)-4-ethoxyphenylphosphine oxide, bis(2,6-dichlorobenzoyl)-4-propylphenylphosphine oxide, bis(2,6-dichlorobenzoyl)-2-naphthylphosphine oxide, bis(2,6-dichlorobenzoyl)-1-naphthylphosphine oxide, bis(2,6-dichlorobenzoyl)-4-chlorophenylphosphine oxide, bis(2,6-dichlorobenzoyl)-2,4-dimethoxyphenylphosphine oxide, bis(2,6-dichlorobenzoyl)decylphosphine oxide, bis(2,6-dichlorobenzoyl)-4-octylphenylphosphine oxide, bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide, bis(2,4,6-trimethylbenzoyl)-2,5-dimethylphenylphosphine oxide, bis(2,6-dichloro-3,4,5-trimethoxybenzoyl)-2,5-dimethylphenylphosphine oxide, bis(2,6-dichloro-3,4,5-trimethoxybenzoyl)-4-ethoxyphenylphosphine oxide, bis(2-methyl-1-naphthoyl)-2,5-dimethylphenylphosphine oxide, bis(2-methyl-1-naphthoyl)-4-ethoxyphenylphosphine oxide, bis(2-methyl-1-naphthoyl)-2-naphthylphosphine oxide, bis(2-methyl-1-naphthoyl)-4-propylphenylphosphine oxide, bis(2-methyl-1-naphthoyl)-2,5-dimethylphenylphosphine oxide, bis(2-methoxy-1-naphthoyl)-4-ethoxyphenylphosphine oxide, bis(2-chloro-1-naphthoyl)-2,5-dimethylphenylphosphine oxide, and bis(2,6-dimethoxybenzoyl)-2,4,4-trimethylpentylphenylphosphine oxide.

Among them, as the acylphosphine oxide compound in the present disclosure, bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide (IRGACURE 819: manufactured by BASF SE), bis(2,6-dimethoxybenzoyl)-2,4,4-trimethylpentylphenylphosphine oxide, 2,4,6-trimethylbenzoyldiphenylphosphine oxide (DAROCUR TPO: manufactured by BASF SE, LUCIRIN TPO: manufactured by BASF SE), 1-[4-(2-hydroxyethoxy)phenyl]-2-hydroxy-2-methyl-1-propane-1-one (IRGACURE 2959: manufactured by BASF SE), and the like are preferable.

The photopolymerization initiator may be used singly or in combination of two or more thereof. In addition, as long as the effects of the liquid composition according to the embodiment of the present disclosure are not impaired, a known sensitizer for the purpose of improving sensitivity can be used in combination.

The ink jet liquid composition according to the embodiment of the present disclosure may contain, as the photopolymerization initiator, a compound that functions as a sensitizer (hereinafter also simply referred to as a “sensitizer”) in order to absorb a specific actinic ray to promote decomposition of the photopolymerization initiator.

Examples of the sensitizer include polynuclear aromatic compounds (such as pyrene, perylene, triphenylene, and 2-ethyl-9,10-dimethoxy anthracene), xanthenes (such as fluorescein, eosin, erythrosine, rhodamine B, and rose bengal), cyanines (such as thiacarbocyanine, and oxacarbocyanine), merocyanines (such as merocyanine, and carbomerocyanine), thiazines (such as thionine, methylene blue, and toluidine blue), acridines (such as acridine orange, chloroflavin, and acriflavine), anthraquinones (such as anthraquinone), squaryliums (such as squarylium), and coumarins (such as 7-diethylamino-4-methylcoumarin).

The sensitizer may be used singly or in a combination of two or more thereof.

The content of the photopolymerization initiator in the ink jet liquid composition according to the embodiment of the present disclosure is preferably 0.1% by mass to 20.0% by mass, more preferably 0.5% by mass to 18.0% by mass, and even more preferably 1.0% by mass to 15.0% by mass with respect to the total mass of the liquid composition. A case where the amount of the polymerization initiator added is in the above range is suitable from the viewpoint of excellent curability and reduction of sticky feeling of the surface.

In addition, the content ratio (mass ratio) between the polymerization initiator and the polymerizable compound to be used in combination (polymerization initiator:polymerizable compound) is preferably 0.5:100 to 30:100, more preferably 1:100 to 15:100, and even more preferably 2:100 to 10:100, respectively.

<Vinyl Chloride-Vinyl Acetate Copolymer>

It is preferable that the ink jet liquid composition according to the embodiment of the present disclosure contains a vinyl chloride-vinyl acetate copolymer (also referred to as a “specific copolymer”).

The vinyl chloride-vinyl acetate copolymer in the present disclosure does not have a polymerizable group.

The copolymerization ratio in the vinyl chloride-vinyl acetate copolymer in the present disclosure is not particularly limited, but from the viewpoint of ink jet jettability, the copolymerization amount of vinyl chloride is preferably 70% by mass to 95% by mass, the copolymerization amount of vinyl acetate is preferably 5% by mass to 30% by mass, the copolymerization amount of vinyl chloride is more preferably 80% by mass to 93% by mass, the copolymerization amount of vinyl acetate is more preferably 7% by mass to 20% by mass, the copolymerization amount of vinyl chloride is particularly preferably 80% by mass to 90% by mass, and the copolymerization amount of vinyl acetate is particularly preferably 10% by mass to 20% by mass.

The weight-average molecular weight (Mw) of the vinyl chloride-vinyl acetate copolymer is preferably 5,000 or more and 100,000 or less, more preferably 10,000 or more and 70,000 or less, and even more preferably 12,000 or more and 50,000 or less from the viewpoint of ink jet jettability.

As the vinyl chloride-vinyl acetate copolymer, a commercially available product may be used.

Examples of the commercially available product include a vinyl chloride-vinyl acetate copolymer manufactured by Wacker Chemie Gmbh, and SOLBIN CL, CNL, C5R, TA3, and TA5R manufactured by Nissin Chemical co., ltd.

The vinyl chloride-vinyl acetate copolymer may be used singly or in a combination of two or more thereof.

The content of the vinyl chloride-vinyl acetate copolymer in the ink jet liquid composition according to the embodiment of the present disclosure is preferably 0.1% by mass or more and 10% by mass or less, more preferably 0.5% by mass or more and 5% by mass or less, and particularly preferably 1% by mass or more and 3% by mass or less with respect to the total mass of the liquid composition from the viewpoint of ink jet jettability and the abrasion resistance and the chemical resistance of the obtained cured film.

<Colorant>

In a case where the ink jet liquid composition according to the embodiment of the present disclosure is used for applications for an ink composition or the like, the ink jet liquid composition may contain a colorant, but it is preferable that the liquid composition does not contain a colorant.

In the present disclosure, the expression “does not contain a colorant” means that a small amount of contamination or the like is allowed, and the ink jet liquid composition does not completely contain the colorant or the content of the colorant is more than 0% by mass and 0.1% by mass or less with respect to the total mass of the composition. In addition, in a case where the ink jet liquid composition is used for applications of a clear ink composition or the like, it is preferable that the ink jet liquid composition does not contain the colorant at all or the content of the colorant is more than 0% by mass and 0.05% by mass or less with respect to the total mass of the composition and it is more preferable that the ink jet liquid composition does not contain the colorant at all or the content of the colorant is more than 0% by mass and 0.01% by mass or less with respect to the total mass of the composition.

The colorant is not particularly limited and pigments and oil-soluble dyes which are excellent in weather fastness and rich in color reproducibility are preferable. The colorant can be randomly selected from known colorants such as soluble dyes and used. As the colorant, it is preferable to select a compound which does not function as a polymerization inhibitor from the viewpoint of not lowering the sensitivity of the curing reaction by active radiation.

The pigment is not particularly limited and can be selected appropriately according to the purpose. Examples thereof include known organic pigments and inorganic pigments, and resin particles dyed with a dye, commercially available pigment dispersions, and surface-treated pigments (for example, a dispersion of a pigment in an insoluble resin, or the like, as a dispersion medium, or a pigment having a resin grafted on the surface) may be used. Examples of these pigments include pigments described in, for example, “Pigment Dictionary”, edited by Seishiro Ito (2000), “Industrial Organic Pigments” edited by W. Herbst, K. Hunger, JP2002-012607A, JP2002-188025A, JP2003-026978A, and JP2003-342503A.

Examples of the organic pigments and inorganic pigments include yellow pigments, magenta pigments, cyan pigments, green pigments, orange pigments, brown pigments, violet pigments, black pigments and white pigments.

The yellow pigments are pigments exhibiting yellow color, and examples thereof include monoazo pigments such as C.I. Pigment Yellow 1 (Fast Yellow G and the like), and C.I. Pigment Yellow 74, disazo pigments such as C.I. Pigment Yellow 12 (Disazo Yellow and the like), C.I. Pigment Yellow 17, C.I. Pigment Yellow 97, C.I. Pigment Yellow 3, C.I. Pigment Yellow 16, C.I. Pigment Yellow 83, C.I. Pigment Yellow 155, and C.I. Pigment Yellow 219, non-benzidine-based azo pigments such as C.I. Pigment Yellow 180, azo lake pigments such as C.I. Pigment Yellow 100 (Tartrazine Yellow Lake and the like), condensed azo pigments such as C.I. Pigment Yellow 95 (Condensed Azo Yellow and the like), C.I. Pigment Yellow 93, C.I. Pigment Yellow 94, C.I. Pigment Yellow 128, and C.I. Pigment Yellow 166, acid dye lake pigments such as C.I. Pigment Yellow 115 (Quinoline Yellow Lake and the like), basic dye lake pigments such as C.I. Pigment Yellow 18 (Thioflavine Lake and the like), anthraquinone pigments such as C.I. Pigment Yellow 24 (Flavanthrone Yellow and the like), quinophthalone pigments such as C.I. Pigment Yellow 110 (Quinophthalone Yellow and the like), isoindoline pigments such as C.I. Pigment Yellow 139 (Isoindoline Yellow and the like), pyrazolone pigments such as C.I. Pigment Yellow 60 (Pyrazolone Yellow and the like), acetolone pigments such as C.I. Pigment Yellow 120, C.I. Pigment Yellow 154, C.I. Pigment Yellow 167, C.I. Pigment Yellow 151, C.I. Pigment Yellow 175, C.I. Pigment Yellow 180, C.I. Pigment Yellow 181, C.I. Pigment Yellow 185, and C.I. Pigment Yellow 194, metal complex salt pigments such as C.I. Pigment Yellow 150, nitroso pigments such as C.I. Pigment Yellow 153 (Nickel Nitroso Yellow and the like), and metal complex salt azomethine pigments such as C.I. Pigment Yellow 117 (Copper Azomethine Yellow and the like).

The magenta pigments are pigments exhibiting red or magenta color, and examples thereof include monoazo-based pigments such as C.I. Pigment Red 3 (Toluidine Red and the like), B-naphthol pigments such as C.I. Pigment Red 1, C.I. Pigment Red 4, and C.I. Pigment Red 6, disazo pigments such as C.I. Pigment Red 38 (Pyrazolone Red B and the like), azo lake pigments such as C.I. Pigment Red 53:1 (Lake Red C and the like), C.I. Pigment Red 57:1 (Brilliant Carmine 6B and the like), C.I. Pigment Red 52:1, and C.I. Pigment Red 48 (B-oxynaththoic acid lake and the like), condensed azo pigments such as C.I. Pigment Red 144, C.I. Pigment Red 166, C.I. Pigment Red 220, C.I. Pigment Red 214, C.I. Pigment Red 221, and C.I. Pigment Red 242 (Condensed Azo Red and the like), acid dye lake pigments such as C.I. Pigment Red 174 (Phloxine B Lake and the like), and the C.I. Pigment Red 172 (Erythrosine Lake and the like), basic dye lake pigments such as C.I. Pigment Red 81 (Rhodamine 6G′ Lake and the like), anthraquinone-based pigments such as C.I. Pigment Red 177 (Dianthraquiononyl Red and the like), thioindigo pigments such as C.I. Pigment Red 88 (Thioindigo Bordeaux and the like), perinone pigments such as C.I. Pigment Red 194 (Perinone Red and the like), perylene pigments such as C.I. Pigment Red 149, C.I. Pigment Red 179, C.I. Pigment Red 178, C.I. Pigment Red 190, C.I. Pigment Red 224, and C.I. Pigment Red 123, quinacridone pigments such as C.I. Pigment Violet 19 (unsubstituted quinacridone), C.I. Pigment Red 122, C.I. Pigment Red 262, C.I. Pigment Red 207, and C.I. Pigment Red 209, isoindolinone pigments such as C.I. Pigment Red 180 (Isoindolinone Red 2BLT and the like), alizarin lake pigments such as C.I. Pigment Red 83 (Madder Lake and the like), naphtholone pigments such as C.I. Pigment Red 171, C.I. Pigment Red 175, C.I. Pigment Red 176, C.I. Pigment Red 185, and C.I. Pigment Red 208, naphthol AS-based lake pigments such as C.I. Pigment Red 247, naphthol AS pigments such as C.I. Pigment Red 2, C.I. Pigment Red 5, C.I. Pigment Red 21, C.I. Pigment Red 170, C.I. Pigment Red 187, C.I. Pigment Red 256, C.I. Pigment Red 268, and C.I. Pigment Red 269, and diketopyrrolopyrrole pigments such as C.I. Pigment Red 254, C.I. Pigment Red 255, C.I. Pigment Red 264, and C.I. Pigment Red 272.

The cyan pigments are pigments exhibiting blue or cyan color, and examples thereof include disazo-based pigments such as C.I. Pigment Blue 25 (Dianisidine Blue and the like), phthalocyanine pigments such as C.I. Pigment Blue 15, C.I. Pigment Blue 15:1, C.I. Pigment Blue 15:2, C.I. Pigment Blue 15:3, C.I. Pigment Blue 15:4, C.I. Pigment Blue 15:6, C.I. Pigment Blue 16 (Phthalocyanine Blue and the like), acid dye lake pigments such as C.I. Pigment Blue 24 (Peacock Blue Lake and the like), basic dye lake pigments such as C.I. Pigment Blue 1 (Victoria Pure Blue BO Lake and the like), anthraquinone-based pigments such as C.I. Pigment Blue 60 (Indanthrone Blue and the like), and alkali blue pigments such as C.I. Pigment Blue 18 (Alkali Blue V-5:1).

The green pigments are pigments exhibiting green color, and examples thereof include phthalocyanine pigments such as C.I. Pigment Green 7 (Phthalocyanine Green), and C.I. Pigment Green 36 (Phthalocyanine Green), and azo metal complex pigments such as C.I. Pigment Green 8, and C.I. Pigment Green 10.

The orange pigments are pigment exhibiting orange color, and examples thereof include isoindoline-based pigments such as C.I. Pigment Orange 66 (Isoindoline Orange), anthraquinone-based pigments such as C.I. Pigment Orange 51 (Dichloro Pyranthorone Orange), B-naphthol pigments such as C.I. Pigment Orange 2, C.I. Pigment Orange 3, and C.I. Pigment Orange 5, naphthol AS pigments such as C.I. Pigment Orange 4, C.I. Pigment Orange 22, C.I. Pigment Orange 24, C.I. Pigment Orange 38, and C.I. Pigment Orange 74, isoindolinone pigments such as C.I. Pigment Orange 61, perinone pigments such as C.I. Pigment Orange 43, disazo pigments such as C.I. Pigment Orange 15 and C.I. Pigment Orange 16, quinacridone pigments such as C.I. Pigment Orange 48, and C.I. Pigment Orange 49, acetolone pigments such as C.I. Pigment Orange 36, C.I. Pigment Orange 62, C.I. Pigment Orange 60, C.I. Pigment Orange 64, and C.I. Pigment Orange 72, and Pyrazolone pigments such as C.I. Pigment Orange 13, and C.I. Pigment Orange 34.

The brown pigments are pigments exhibiting brown color, and examples thereof include naphtholone pigments such as C.I. Pigment Brown 25 and C.I. Pigment Brown 32.

The violet pigments are pigments exhibiting purple color, and examples thereof include naphtholone pigments such as C.I. Pigment Violet 32, perylene pigments such as C.I. Pigment Violet 29, naphthol AS pigments such as C.I. Pigment Violet 13, C.I. Pigment Violet 17, and C.I. Pigment Violet 50, and dioxazine pigments such as C.I. Pigment Violet 23 and C.I. Pigment Violet 37.

The black pigments are pigments exhibiting black color, and examples thereof include carbon black such as MOGUL E, titanium black, indazine pigments such as and the C.I. Pigment Black 1 (Aniline Black), and perylene pigments such as C.I. Pigment Black 31, and C.I. Pigment Black 32.

Examples of the white pigments include basic lead carbonate (2PbCO₃Pb(OH)₂, a so-called silver white), zinc oxide (ZnO, a so-called zinc white), titanium oxide (TiO₂, a so-called titanium white), and strontium titanate (SrTiO₃, a so-called a titanium strontium white). Inorganic particles used for a white pigment may be a simple substance, or may be complex particles with oxides of silicon, aluminum, zirconium or titanium, or with organometallic compounds and an organic compound.

Among them, since titanium oxide has a low specific gravity as compared with other white pigments and has a high refractive index, is chemically and physically stable, and is excellent in the covering power and adhesion as a pigment, and further, the durability in acidic, alkaline and other environments, titanium oxide is suitably used. Other white pigments (may be white pigments other than the above white pigments) may be used together with titanium oxide in combination.

For the dispersion of the pigment, for example, dispersion apparatuses such as a ball mill, a sand mill, an attritor, a roll mill, a jet mill, a homogenizer, a paint shaker, a kneader, an agitator, a HENSCHEL mixer, a colloid mill, an ultrasound homogenizer, a pearl mill, a wet-type jet mill, and the like can be suitably used.

In the present disclosure, a dispersant to be described later is preferably added upon dispersion of the pigment.

In addition, upon dispersion of the pigment, if necessary, a synergist according to various pigments may be added as a dispersion aid. The content of the dispersion aid in the liquid composition is preferably 1 part by mass to 50 parts by mass with respect to 100 parts by mass of the pigment.

The dispersion medium used in a case where the pigment is dispersed in the liquid composition is not particularly limited and can be appropriately selected according to the purpose. For example, the polymerizable compound with a low molecular weight may be used as the dispersion medium, or a solvent is used as the dispersion medium. However, since the ink jet liquid composition according to the embodiment of the present disclosure is a radiation curable-type polymerizable composition and, for example, the liquid composition is cured after the polymerizable composition is applied onto a recording medium, a solvent-free dispersion medium containing no solvent is preferable. This is because in a case where a solvent remains in the cured product, solvent resistance is deteriorated or problems associated with a volatile organic compound (VOC) of the remaining solvent. Therefore, from the viewpoint of improving the dispersion suitability and handleability of the liquid composition, it is preferable that the polymerizable compounds are used as the dispersion medium and that a polymerizable compound with the lowest viscosity is selected from among these polymerizable compounds.

The average particle diameter of the pigment is not particularly limited and can be appropriately selected according to the purpose. However, since the color developability improves with the decrease in particle diameter, the average particle diameter is preferably about 0.01 μm to 0.4 μm and more preferably 0.02 μm to 0.2 μm. In addition, a particle diameter of 3 μm or less is preferable and 1 μm or less is more preferable as the maximum particle diameter of the pigment. The particle diameter of the pigment can be adjusted by appropriately selecting the pigment, dispersant, and dispersion medium and by setting appropriate dispersion conditions and filtration conditions. By controlling the particle diameter of the pigment, it is possible to prevent a head of nozzle from clogging and maintain preservation stability, transparency, and curing sensitivity.

The particle diameter of the pigment can be measured by a known measurement method. Specifically, the measurement can be performed by a centrifugal sedimentation light transmission method, an X-ray transmission method, a laser diffraction and scattering method, and a dynamic light scattering method.

The colorant may be used singly or in combination of two or more thereof.

In a case where the ink jet liquid composition according to the embodiment of the present disclosure contains the colorant, the content of the colorant in the ink jet liquid composition is appropriately selected according to the color and the purpose of use, but is preferably 0.01% by mass to 20% by mass with respect to the total mass of the composition.

<Dispersant>

The ink jet liquid composition according to the embodiment of the present disclosure may contain a dispersant. Particularly, in a case of using a pigment, since the pigment is stably dispersed in the composition, it is preferable to contain a dispersant. The dispersant is preferably a polymer dispersant. The term “polymer dispersant” in the present disclosure means a dispersant having a weight-average molecular weight of 1,000 or more.

Examples of the polymer dispersant include DISPERBYK-101, DISPERBYK-102, DISPERBYK-103, DISPERBYK-106, DISPERBYK-111, DISPERBYK-161, DISPERBYK-162, DISPERBYK-163, DISPERBYK-164, DISPERBYK-166, DISPERBYK-167, DISPERBYK-168, DISPERBYK-170, DISPERBYK-171, DISPERBYK-174, and DISPERBYK-182 (manufactured by BYK Chemie GmbH)); EFKA4010, EFKA4046, EFKA4080, EFKA5010, EFKA5207, EFKA5244, EFKA6745, EFKA6750, EFKA7414, EFKA745, EFKA7462, EFKA7500, EFKA7570, EFKA7575, EFKA7580, and EFKA7701 (manufactured by EFKA Additives Co., Ltd.); DISPERSE AID 6, DISPERSE AID 8, DISPERSE AID 15, and DISPERSE AID 9100 (manufactured by San Nopco Co., Ltd.); various SOLSPERSE dispersants such as SOLSPERSE 3000, 5000, 9000, 12000, 13240, 13940, 17000, 22000, 24000, 26000, 28000, 32000, 36000, 39000, 41000, and 71000 (manufactured by Noveon, Inc.); ADEKA PLURONIC L31, F38, L42, L44, L61, L64, F68, L72, P95, F77, P84, F87, P94, L101, P103, F108, L121, and P-123 (manufactured by ADEKA Ltd.), IONETTO S-20 (manufactured by Sanyo Chemical Industries, Ltd.); DISPARLON KS-860, 873SN, and 874 (polymer dispersant), #2150 (aliphatic polyvalent carboxylic acid), and #7004 (polyether ester type) (manufactured by Kusumoto Kasei Co., Ltd.).

The dispersant may be used singly or in combination of two or more thereof.

The content of the dispersant in the liquid composition according to the embodiment of the present disclosure is appropriately selected according to the purpose of use and is preferably 0.05% by mass to 10% by mass with respect to the total mass of the liquid composition.

<Other Components>

To the ink jet liquid composition according to the embodiment of the present disclosure, in addition to the above-described components, if necessary, known additives such as a polymerization inhibitor, an ultraviolet absorber, an antioxidant, an antifading agent, a surface conditioner, a leveling agent, a matting agent, a wax, an antifoaming agent, a pH adjuster, a charge imparting agent, a disinfectant, a preservative, a deodorant, a charge controlling agent, a wetting agent, an antiskinning agent, a fragrance, and a pigment derivative may be added as an arbitrary component.

The ink jet liquid composition according to the embodiment of the present disclosure preferably contains a polymerization inhibitor from the viewpoint of improving storability and suppressing clogging of an ink jet head.

The content of the polymerization inhibitor is preferably 200 ppm to 20,000 ppm with respect to the total mass of the composition.

Examples of the polymerization inhibitor include nitroso-based polymerization inhibitors, hindered amine-based polymerization inhibitors, hydroquinone, benzoquinone, p-methoxy phenol, TEMPO, TEMPOL, and CUPERON A1.

<Physical Properties of Ink Jet Liquid Composition>

The viscosity of the ink jet liquid composition according to the embodiment of the present disclosure at 25° C. is preferably 1 mPa·s to 40 mPa·s, and more preferably 3 mPa·s to 30 mPa·s.

In addition, the viscosity at the temperature at the time of ink jetting (preferably 25° C. to 80° C., more preferably 25° C. to 50° C.) is preferably 1 mPa·s to 30 mPa·s and more preferably 3 mPa·s to 25 mPa·s. The ink jet liquid composition that can be used in the present disclosure preferably has the compositional ratio appropriately adjusted such that the viscosity is set to be in the above-described ranges. It is possible to inhibit bleeding when a liquid droplet of the liquid composition lands.

The measurement method of the viscosity is not particularly limited; however, preferable examples include a method using a model RE80 viscometer manufactured by Toki Sangyo Co., Ltd. The model RE80 type viscometer is a conical rotor and flat plate type viscometer corresponding to an E-type, and measurement is preferably performed at a rotation speed of 10 rpm using rotor code No. 1 as a rotor. Herein, measurement is preferably performed by changing the rotation speed to 5 rpm, 2.5 rpm, 1 rpm, 0.5 rpm and the like if necessary for those having a high viscosity higher than 60 mPa·s.

In addition, the surface tension of the ink jet liquid composition according to the embodiment of the present disclosure at 25° C. is preferably 18 mN/m or more and 50 mN/m or less, and more preferably 20 mN/m or more and 40 mN/m or less from the viewpoint of appropriateness of liquid droplet jetting by the ink jet.

In addition, the surface tension of the ink jet liquid composition according to the embodiment of the present disclosure is a value measured at a liquid temperature of 25° C. with the Wilhelmy method using a generally used surface tensiometer (for example, a CBVP-Z surface tensiometer, manufactured by Kyowa Interface Science Co., Ltd., or the like).

(Ink Jet Recording Method)

An ink jet recording method according to an embodiment of the present disclosure includes a step of applying the ink jet liquid composition according to the embodiment of the present disclosure to a base material by an ink jet recording head.

The base material is preferably a base material having a concave-convex shape in at least a part of the surface and more preferably leather from the viewpoint of further exerting the effects of ink jet liquid composition according to the embodiment of the present disclosure.

In the step of the applying, the liquid composition may be directly applied to the base material or a layer such as a decorative layer may be provided to the base material and the liquid composition may be applied to the layer.

The ink jet jetting condition and the jetting amount in the step of the applying are not particularly limited and may be appropriately selected according to the composition and physical properties of the liquid composition to be used, the base material, and the like.

In addition, a printed material according to the embodiment of the present disclosure is a printed material having a cured product obtained by curing the ink jet liquid composition according to the embodiment of the present disclosure, and is preferably a printed material on which recording is performed by the ink jet recording method according to the embodiment of the present disclosure.

In the ink jet recording method according to the embodiment of the present disclosure, an ink jet recording apparatus to be described later in detail can be used.

The ink jet recording apparatus that can be used in the ink jet recording method according to the embodiment of the present disclosure is not particularly limited and, a known ink jet recording apparatus capable of achieving a desired resolution can be arbitrarily selected and used. That is, any ink jet recording apparatus can jet the liquid composition to the base material in the ink jet recording method according to the embodiment of the present disclosure as long as the ink jet recording apparatus is a known ink jet recording apparatus including commercially available products.

Examples of the ink jet recording apparatus according to the embodiment of the present disclosure include apparatuses including ink supply systems, temperature sensors, and active radiation sources.

The ink supply system, for example, is formed of a source tank including the liquid composition according to the embodiment of the present disclosure, a supply pipe, an ink supply tank immediately before the ink jet head, a filter, and a piezo type ink jet head. The piezo type ink jet head can perform driving so as to enable jetting multi-size dots of preferably 1 pl to 100 pl, and more preferably 8 pl to 30 pl at a resolution of preferably 320×320 dpi to 4,000×4,000 dpi, more preferably 400×400 dpi to 1,600×1,600 dpi, and even more preferably 720×720 dpi. The term dpi (dot per inch) used in the present disclosure represents the number of dots per 2.54 cm.

As described above, for the liquid composition according to the embodiment of the present disclosure, since it is preferable that the jetted liquid composition is set to a constant temperature, it is preferable that means for stabilizing the liquid composition temperature is provided in the ink jet recording apparatus. As sites made a constant temperature, all of the pipe system and members from the ink tank (the intermediate tank, in a case where there is an intermediate tank) to the nozzle emission surface become targets. That is, insulation and heating can be performed from the ink supply tank to the ink jet head portion.

The temperature control method is not particularly limited; however, for example, it is preferable to provide a plurality of temperature sensors at sites at each pipe and perform heating control according to the flow rate of the liquid composition and the environmental temperature. The temperature sensors can be provided in the vicinity of the ink supply tank and the nozzles of the ink jet head. In addition, the head unit to be heated is preferably thermally blocked or insulated such that the apparatus main body is not influenced by the temperature from the outside air. In order to shorten the printer startup time required for heating, or in order to reduce the thermal energy loss, it is preferable to provide insulation from other sites and to decrease the heat capacity of the entire heating unit body.

In addition, it is preferable to keep the temperature of the liquid composition during jetting as constant as possible. The control range of the temperature of the liquid composition during jetting is set to preferably ±5° C. of a set temperature, more preferably ±2° C., and even more preferably ±1° C. is appropriate.

In addition, it is preferable that the ink jet recording method according to the embodiment of the present disclosure further includes a step of drying the ink jet liquid composition on the base material by applying heat; and a step of curing the ink jet liquid composition by irradiating the ink jet liquid composition with active radiation.

In the ink jet recording method according to the embodiment of the present disclosure, the liquid composition may be dried by air or may be dried by applying heat, but is preferably dried by applying heat.

The drying temperature in the step of the drying is not particularly limited and may be appropriately set according to the boiling point of the organic solvent in the liquid composition. The base material temperature is preferably 30° C. or higher and 90° C. or lower and more preferably 50° C. or higher and 80° C. or lower.

Next, the irradiation with active radiation will be described.

The dried liquid composition on the base material is cured by being irradiated with active radiation. This is because the polymerization initiator included in the liquid composition according to the embodiment of the present disclosure generates polymerization initiating species, such as radicals by decomposing due to irradiation with active radiation, and the polymerization reaction of the polymerizable compound is started and promoted by the function of the initiating species. At this time, in a case where a sensitizer is present along with a polymerization initiator in the liquid composition, the sensitizer in the system absorbs active radiation and enters an excited state, the decomposition of the polymerization initiator is promoted by the contact with the sensitizer, and a curing reaction with a higher sensitivity can be attained.

Here, the active radiation used can be an α-ray, a γ-ray, an electron beam, an X-ray, an ultraviolet (UV) ray, visible light or infrared light. The peak wavelength of the active radiation also depends on the absorption characteristics of the sensitizer. However, the peak wavelength is preferably 200 nm to 600 nm, more preferably 300 nm to 450 nm, and even more preferably 320 nm to 420 nm, and the active energy ray is particularly preferably an ultraviolet ray with a peak wavelength in a range of 340 nm to 400 nm.

In addition, the polymerization initiation system of the liquid composition according to the embodiment of the present disclosure has sufficient sensitivity even with a low output active energy ray. Accordingly, curing is suitably performed with an exposure surface illuminance of preferably 10 mW/cm² to 4,000 mW/cm², and more preferably 20 mW/cm² to 2,500 mW/cm².

As the active radiation source, a mercury lamp, a gas or solid-state laser, or the like is mainly used, and a metal halide lamp is widely known. However, currently, the current move toward becoming mercury free is strongly desired from the viewpoint of environmental protection, and replacement with GaN-based semiconductor ultraviolet light emitting devices is industrially and environmentally extremely effective. Further, LED (UV-LED) and LD (UV-LD) are small size and low cost, and have long service life and high efficiency, and are anticipated as a photocuring type ink jet light source.

In addition, it is possible to use light emitting diodes (LED) and laser diodes (LD) as active radiation sources. In particular, in a case where an ultraviolet source is required, an ultraviolet LED and an ultraviolet LD can be used. For example, Nichia Corporation has brought an ultraviolet LED to market having a wavelength with a main emission spectrum between 365 nm and 420 nm. Furthermore, in a case where an even shorter wavelength is needed, the specification of U.S. Pat. No. 6,084,250A discloses an LED capable of emitting active radiation centered between 300 nm and 370 nm. In addition, other ultraviolet LEDs are available and can emit radiation of different ultraviolet ray bands. In the present disclosure, a UV-LED is a particularly preferable active energy ray source, and particularly preferable is a UV-LED having a peak wavelength of 340 nm to 400 nm.

In addition, the maximum illuminance on the recording medium of the LED is preferably 10 mW/cm² to 2,000 mW/cm², more preferably 20 mW/cm² to 1,000 mW/cm², and particularly preferably 50 mW/cm² to 800 mW/cm².

The ink jet liquid composition according to the embodiment of the present disclosure is suitably irradiated with such active radiation for preferably 0.01 seconds to 120 seconds and more preferably 0.1 seconds to 90 seconds.

The irradiation conditions of the active radiation and the basic irradiation method are disclosed in JP1985-132767A (JP-S60-132767A).

Further, curing may be completed using another light source that is not driven. WO99/054415A as an irradiation method, a method using an optical fiber, and a method of directing a collimated light source to a mirror surface, which is provided on the side surface of a head unit, to irradiate a recorded area with UV light. The above-described curing methods can be applied to the ink jet recording method according to the embodiment of the present disclosure.

Among these, as the ink jet recording method according to the embodiment of the present disclosure, an ink jet recording method including a step of preparing a base material having a decorative layer formed thereon, a step of applying the ink jet liquid composition according to the embodiment of the present disclosure not containing a colorant to the decorative layer by an ink jet recording head, a step of drying the ink jet liquid composition on the decorative layer by applying heat, and a step of curing the ink jet liquid composition by irradiating the ink jet liquid composition with an ultraviolet ray, in which the base material having the decorative layer formed thereon has a concave-convex shape in at least a part of a surface is preferably used.

The decorative layer may be formed using the liquid composition according to the embodiment of the present disclosure as a coloring ink composition or may be formed using a known ink composition.

Among these, an embodiment in which both the decorative layer and the overcoat formed on the decorative layer are formed by the ink jet liquid composition according to the embodiment of the present disclosure is preferable. The above embodiment is particularly preferable for a decorative layer and an overcoat provided on a base material having a concave-convex shape in at least a part of the surface thereof.

By forming an overcoat on the decorative layer using the liquid composition according to the embodiment of the present disclosure, even in a case where a known ink composition is used, abrasion resistance, bendability, and chemical resistance are excellent.

In addition, as the ink jet recording method according to the embodiment of the present disclosure, an ink jet recording method including a step of applying the ink jet liquid composition containing a colorant according to the embodiment of the present disclosure to a base material by an ink jet recording head, a step of drying the ink jet liquid composition on the base material by applying heat, a step of curing the ink jet liquid composition by irradiating the ink jet liquid composition with an ultraviolet ray to form a decorative layer, a step of applying the ink jet liquid composition according to the embodiment of the present disclosure not containing a colorant to the decorative layer by an ink jet recording head, a step of drying the ink jet liquid composition on the decorative layer by applying heat, and a step of curing the ink jet liquid composition by irradiating the ink jet liquid composition with an ultraviolet ray is preferable, and an ink jet recording method in which the base material has a concave-convex shape in at least a part of the surface thereof is more preferable.

As the base material, not only a base material having a concave-convex shape in at least a part of the surface of the above-mentioned leather or the like, but also papers such as ordinary uncoated paper and coated paper, various nonabsorbent resin materials used for so-called soft packaging and resin films formed by molding the resins materials in a film form can also be used.

Examples of the various plastic films include a polyethylene terephthalate (PET) film, a biaxially oriented polystyrene (OPS) film, a biaxially oriented polypropylene (OPP) film, a biaxially oriented nylon (ONy) film, a polyvinyl chloride (PVC) film, a polyethylene (PE) film, and a cellulose triacetate (TAC) film.

In addition, examples of plastics that can be used as the base material include polycarbonate, an acrylic resin, an acrylonitrile-butadiene-styrene (ABS) copolymer, polyacetal, polyvinyl alcohol (PVA), and rubbers. Further, metals and glasses can be used as the recording medium.

EXAMPLES

Hereinafter, the present invention will be more specifically described based on examples, but the present disclosure is not limited to the examples. Herein, unless otherwise specified, “part” and “%” are based on mass.

<L2/L1 in Base Material>

The L2/L1 in the base material was measured using a shape analysis laser microscope (VK-X250/260, manufactured by Keyence Corporation).

Hereinafter, the details of various components used in Examples and Comparative Examples are shown.

-   -   Cyan pigment (PB15:4, C.I. Pigment Blue 15:4, HELIOGEN BLUE D         7110 F, manufactured by BASF SE)     -   Magenta pigment (mixed quinacridone, CINQUASIA MAGENTA L 4540,         manufactured by BASF SE)     -   Yellow pigment (PY155, C.I. Pigment Yellow 155, INK JET YELLOW         4GC, manufactured by Clarinat)     -   Black pigment (carbon black, MOGUL E, manufactured by CABOT)     -   Dispersant (Sol32000, SOLSPERSE 32000, manufactured by The         Lubrizol Corporation)

The details of the organic solvents used in Examples and Comparative Examples are shown in Table 1.

TABLE 1 Boiling Compound name point (° C.) Manufacturer 3-Methoxybutyl acetate 172 Tokyo Chemical Industry Co., Ltd. Triethylene glycol monobutyl 278 Tokyo Chemical Industry ether (TEGMBE) Co., Ltd. Diethylene glycol dimethyl 188 Tokyo Chemical Industry ether (DEGDEE) Co., Ltd.

The details of the urethane (meth)acrylate oligomers (oligomers) used in Examples and Comparative Examples are shown in Table 2.

TABLE 2 Trade name Manufacturer Functional number Mw CN9001 Sartomer Company Inc. Bifunctional 3,250 SHIKO The Nippon Synthetic Hexafunctional 1,400 UV-7600B Chemical Industry Co., Ltd. SHIKO The Nippon Synthetic Bifunctional 5,000 UV-3310B Chemical Industry Co., Ltd. SHIKO The Nippon Synthetic Trifunctional 2,400 UV-7550B Chemical Industry Co., Ltd.

The details of the vinyl chloride-vinyl acetate copolymers used in Examples and Comparative Examples are shown in Table 3.

TABLE 3 Vinyl Vinyl Vinyl chloride- chloride acetate vinyl acetate (% by (% by copolymer mass) mass) Mw Manufacturer vinnol H14/36 85.6 14.4 16,000 Wacker Chemie AG vinnol H11/59 90.5 9.5 43,000 Wacker Chemie AG

-   -   Polymerization inhibitor (UV 22, Irgastab (registered trademark)         UV-22,         Poly[oxy(methyl-1,2-ethanediyl)]-α,α′,α″-1,2,3-propanetriyltris[-[(1-oxo-2-propen-1-yl)oxy]-2,6-bis(1,1-dimethylethyl)-4-(phenylenemethylene)cyclohexa-2,5-dien-1-one],         manufactured by BASF SE)     -   Polymerization inhibitor (UV 12, nitroso-based polymerization         inhibitor, tirs(N-nitroso-N-phenylhydroxylamine) aluminum salt,         FLORSTAB UV12, manufactured by Kromachem Co., Ltd.)     -   Photopolymerization initiator (Irg819,         bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide, IRGACURE         (registered trademark) 819, manufactured by BASF SE)     -   Photopolymerization initiator (Irg2959, 1-[4-(2-hydroxyethoxy)         phenyl]-2-hydroxy-2-methyl-1-propane-1-one, IRGACURE (registered         trademark) 2959, manufactured by BASF SE)     -   Monomer (PEA, 2-phenoxyethyl acrylate, SR339C, manufactured by         Sartomer Company Inc.)     -   KP109 (50% sol.) (50% by mass propylene glycol monomethyl ether         solution of polyether-modified siloxane compound, manufactured         by Shin-Etsu Chemical Co., Ltd., Mw 12,000, content of siloxane         structure: 29% by mass)     -   KP368 (polyether-modified siloxane compound, manufactured by         Shin-Etsu Chemical Co., Ltd., Mw 7,000, content of siloxane         structure: 90% by mass or more)     -   KP306 (polyether-modified siloxane compound, manufactured by         Shin-Etsu Chemical Co., Ltd., Mw 12,000, content of siloxane         structure: 25% by mass)     -   KP341 (polyether-modified siloxane compound, manufactured by         Shin-Etsu Chemical Co., Ltd., Mw 11,000, content of siloxane         structure: 15% by mass)     -   KF-96H-10,000 CS (polyether-modified siloxane compound,         manufactured by Shin-Etsu Chemical Co., Ltd., Mw70,000, content         of siloxane structure: 20% by mass or more)     -   KF-96H-30,000 CS (polyether-modified siloxane compound,         manufactured by Shin-Etsu Chemical Co., Ltd., Mw 90,000, content         of siloxane structure: 20% by mass or more)     -   KF-96H-100,000 CS (polyether-modified siloxane compound,         manufactured by Shin-Etsu Chemical Co., Ltd., Mw 100,000,         content of siloxane structure: 20 by mass or more)     -   BYK-UV 3500 (polyether modified polydimethylsiloxane,         manufactured by BYK Chemie GmbH, Mw 3,500, content of siloxane         structure: 30% by mass or more)     -   BYK 331 (polyether-modified polydimethylsiloxane, manufactured         by BYK Chemie GmbH, Mw 2,500, content of siloxane structure: 10%         by mass)     -   Efka SL 3210 (polyether-modified siloxane compound, manufactured         by Efka Chemicals, Mw 1,500, content of siloxane structure: 9%         by mass)     -   KP105 (30% sol.) (30% by mass propylene glycol monomethyl ether         solution of polyol-modified siloxane compound, manufactured by         Shin-Etsu Chemical Co., Ltd.)     -   MEGAFACE RS-72-K (40% sol.) (40% by mass methyl isobutyl ketone         solution of fluorine-based surfactant, manufactured by DIC         Corporation)

Examples 1 to 29 and Comparative Examples 1 to 11

<Preparation of Pigment Dispersion>

The compositions other than the pigments shown in Table 4 were mixed and stirred (10 to 15 minutes, 2,000 to 3,000 rpm/min) with a mixer manufactured by SILVERSON Co., Ltd. to obtain a homogenous colorless liquid (diluted solution of dispersant). The pigments were added to the colorless liquid (diluted solution of dispersant), and further stirred with the mixer (10 to 20 minutes, 2,000 to 3,000 rpm/min) to obtain 500 parts of a homogenous preliminary dispersion liquid. Thereafter, a dispersion process was performed using a circulation bead mill device (SL-012C1) manufactured by EIGER Corp. Dispersion was performed under dispersion conditions in which 200 parts of zirconia beads with a diameter of 0.65 mm were charged, and the circumferential speed was set to 15 m/s. The dispersion time was set to 1 to 6 hours.

TABLE 4 Cyan Magenta Yellow Black pigment pigment pigment pigment mill base mill base mill base mill base Pigment PB15:4 Mixed PY155 Carbon black quinacridone 30% by mass 30% by mass 30% by mass 30% by mass Dispersant Sol32000 Sol32000 Sol32000 Sol32000 10% by mass 15% by mass 10% by mass 10% by mass DEGDEE 60% by mass 55% by mass 60% by mass 60% by mass

<Preparation of Coloring Liquid Composition>

The composition shown in Table 5 was mixed and stirred using a mixer manufactured by SILVERSON Machines, Inc. (10 to 15 minutes, 2,000 to 3,000 rotations/min) to prepare a homogenous coloring liquid composition. This composition was used as a coloring liquid composition for Pattern 2 described later.

TABLE 5 Coloring liquid composition C1 M1 Y1 K1 Organic solvent 3-Methoxybutyl 79.9 74.7 75.9 78.4 acetate Oligomer CN9001 7 7 7 7 Resin vinnol H14/36 3 3 3 3 Polymerization UV22 1 1 1 1 inhibitor Photopolymerization Irg819 2 2 2 2 initiator Irg2959 1 1 1 1 Surfactant BYK 331 0.1 0.1 0.1 0.1 Cyan pigment mill base 6 — — — Magenta pigment mill base — 11.2 — — Yellow pigment mill base — — 10 — Black pigment mill base — — — 7.5

<Preparation of Ink Jet Liquid Composition>

Each compound and the like were mixed at the composition in each of Tables 6 to 9 shown below and stirred (10 to 15 minutes, 2,000 to 3,000 rpm/min), with a mixer manufactured by SILVERSON Co., Ltd., to obtain a homogenous ink jet liquid composition.

<Ink Jet Recording Method>

To an ink jet printer (KEGON) manufactured by Afit Corporation, a rubber heater (SR100, manufactured by ThreeHigh Co., Ltd.) and an ultraviolet (UV) irradiation apparatus (Vzero, manufactured by Integration Technology) were attached. The output of the rubber heater was set such that the temperature of the base material could be increased to about 60° C. In addition, the time from ink jet jetting to UV exposure corresponded to the drying time of the liquid droplet and the transfer speed (5 m/min to 25 m/min) and the timing of opening or closing the UV shutter were adjusted such that the time was set to 10 seconds.

Printing was carried out with the configuration of two patterns. Each configuration is as shown below.

—Printing Pattern 1 (Single Layer)—

By jetting the coloring liquid composition from an ink jet head heated to 35° C., printing was performed on the base material (unless otherwise specified, PVC leather (ARES YP606, manufactured by YAMAPLAS CO., LTD., polyvinyl chloride synthetic leather, L2/L1=1.33) was used). At this time, the image density was set to 1,200 dpi×600 dpi and the amount of the coloring liquid compositions applied (total amount of all colors) to the base material was set to 20 g/m².

After the printing, the temperature was raised to 60° C. (base material temperature) by a rubber heater. The drying time was set to 60 seconds.

After drying, exposure was performed in an irradiation amount of 3,000 mJ/cm² by a UV exposure machine to form a decorative layer.

—Printing Pattern 2—

By jetting the coloring liquid composition from an ink jet head heated to 35° C., printing was performed on the base material (unless otherwise specified, PVC leather (ARES YP606, manufactured by YAMAPLAS CO., LTD., polyvinyl chloride synthetic leather, L2/L1=1.33) was used). At this time, the image density was set to 1,200 dpi×600 dpi and the amount of the coloring liquid compositions applied (total amount of all colors) to the base material was set to 20 g/m².

After the printing, the temperature was raised to 60° C. (base material temperature) by a rubber heater. The drying time was set to 60 seconds.

After drying, exposure was performed in an irradiation amount of 3,000 mJ/cm² by a UV exposure machine to form a decorative layer.

A transparent liquid composition was jetted from the ink jet head heated to 35° C. to this decorative layer. At this time, the image density was set to 1,200 dpi×600 dpi and the amount of the transparent liquid compositions applied to the base material was set to 10 g/m².

After the jetting, the temperature was raised to 60° C. (base material temperature) by a rubber heater. The drying time was set to 10 seconds.

After drying, exposure was performed in an irradiation amount of 3,000 mJ/cm² by a UV exposure machine to form a protective layer.

1. Printing of Printing Pattern 1 with Coloring Liquid Composition

Each liquid composition shown in Table 8 or 9 was introduced into the ink jet printer and the pattern 1 was printed.

Each of rectangular solid images of 20 cm×12 cm was printed to form a cured image. The abrasion resistance, bendability, and chemical resistance were evaluated using the cured image based on the evaluation standards described later. The evaluation results are collectively shown in Table 8 or 9.

2. Printing of Printing Pattern 2 with Transparent Liquid Composition

Each liquid composition shown in Tables 6 to 9 was introduced into the ink jet printer and the pattern 2 was printed. As the coloring liquid composition, a set of C1, M1, Y1, and K1 was used. A yellow solid image of a size of 20 cm×12 cm was printed and a base material having a decorative layer formed thereon was prepared. Each of the transparent liquid compositions shown in Tables 6 to 9 was used as a transparent liquid composition to form a protective layer on the decorative layer. The abrasion resistance, bendability, and chemical resistance were evaluated for the prepared samples according to the following evaluation standards.

The evaluation results are collectively shown in Tables 6 to 9.

<Evaluation>

(Abrasion Resistance)

Using a gakushin type tester (manufactured by Suga Test Instruments Co., Ltd.), a certain number of times of abrasion was carried out on the above cured image while applying a load of 200 g by dried cotton (white cloth for test: cotton (Kanakin No. 3, purchased from Japan Standard Association)). During this period, the number of times of abrasion until scratches were visually recognized on the cured image was recorded and the abrasion resistance of the cured image was evaluated according to the following evaluation standards. 3 points or higher in the following evaluation standards are considered as a pass.

—Evaluation Standards of Abrasion Resistance—

5 points: No scratches were generated even at 2,000 times of abrasion.

4 points: Scratches were generated at 1,000 times or more and less than 2,000 times of abrasion.

3 points: Scratches were generated at 500 times or more and less than 1,000 times of abrasion.

2 points: Scratches were generated at 100 times or more and less than 500 of abrasion.

1 point: Scratches were generated at less than 100 times of abrasion.

(Bendability)

Using a bending tester (Flexiometer, manufactured by Yasuda Seiki Seisakusho, Ltd.), a certain number of times of bending was performed on the base material on which the cured image was formed. During this period, the number of times until cracks were visually recognized in the cured image was recorded and the bendability of the cured image was evaluated according to the following evaluation standards. 3 points or higher in the following evaluation standards are considered as a pass.

—Evaluation Standards of Bendability—

5 points: No cracks were generated even at 20,000 times of bending.

4 points: Cracks were generated at 10,000 times or more and less than 20,000 times of bending.

3 points: Cracks were generated at 5,000 times or more and less than 10,000 of bending.

2 points: Cracks were generated at 1,000 times or more and less than 5,000 times of bending.

1 point: Cracks were generated at less than 1,000 of times of bending.

(Chemical Resistance)

Using a gakushin type tester (manufactured by Suga Test Instruments Co., Ltd.), a certain number of times of abrasion was carried out on the above cured image, while applying a load of 400 g by cotton impregnated with ethanol (white cloth for test: cotton (Kanakin No. 3, purchased from Japan Standard Association)). During this period, the cured image was peeled off, the number of times until surface of the base material was visually recognized was recorded and the chemical resistance of the cured image was evaluated according to the following evaluation standards. 3 points or higher in the following evaluation standards are considered as a pass.

—Evaluation Standards of Chemical Resistance—

5 points: The surface of the base material was not visually recognized even at 200 times of abrasion.

4 points: The surface of the base material was visually recognized at 100 times or more and less than 200 times of abrasion.

3 points: The surface of the base material was visually recognized at 50 times or more and less than 100 times of abrasion.

2 points: The surface of the base material was visually recognized at 10 times or more and less than 50 of abrasion.

1 point: The surface of the base material was visually recognized at less than 10 times of abrasion.

(Adhesiveness)

The cured image was subjected to a cross cut test according to JIS K 5066-5-6: 1992. The operation (hereinafter, referred to as “peeling operation”) until the tape was attached to the cross-cut portion of the cured image and was peeled off was performed three times. During this time, the portion subjected to the peeling operation was visually observed, and the adhesiveness of the cured image was evaluated according to the following evaluation standards. 3 points or higher in the following evaluation standards are considered as a pass.

—Evaluation Standards of Adhesiveness—

5 points: The cured image was not damaged by three peeling operations.

4 points: The cured image was damaged by the third peeling operation.

3 points: The cured image was damaged by the second peeling operation.

2 points: The cured image was damaged by the first peeling operation. (however, the image was not peeled off).

1 point: The cured image was damaged and peeled off by the first peeling operation.

(Ink Jet (IJ) Jetting Stability)

Under the same solid image printing conditions except that the base material was changed to an A3 size recording sheet (GASAI, ink jet photographic printing paper, manufactured by Fujifilm Corporation), continuous solid image printing was performed on 40 recording sheet. Hereinafter, a recording sheet on which a solid image is printed is referred to as a “sample”. 40 samples were visually observed and the number of samples in which nozzle missing (that is, an image defect due to nozzle jetting failure) was confirmed in the solid image was examined. Based on this result, ink jet jetting stability was evaluated according to the following evaluation standards. 3 points or higher in the following evaluation standards are considered as a pass.

—Evaluation Standards of Ink Jet Jetting Stability—

5 points: Number of samples in which nozzle missing is confirmed is 0.

4 points: Number of samples in which nozzle missing is confirmed is 1.

3 points: Number of samples in which nozzle missing is confirmed is 2.

2 points: Number of samples in which nozzle missing is confirmed is 3.

1 point: Number of samples in which nozzle missing is confirmed is 4 or more.

TABLE 6 Example 1 2 3 4 5 6 7 8 9 10 Printing pattern 2 2 2 2 2 2 2 2 2 2 Solvent 3-Methoxybutyl acetate 82 81 80 86 83.5 82.5 82.5 82 82 82 Oligomer CN9001 (bifunctional, Mw 3,250) 5 5 5 4 4 4 5 5 5 5 SHIKO UV-7600B (hexafunctional, 5 5 5 4 4 4 5 5 5 5 Mw 1,400) Resin Vinnol H14/36 2 2 2 1 1 1 2 2 2 2 Polymer- UV12 1 1 1 1 1 1 1 1 1 1 ization inhibitor Photopoly- Irg819 3 3 3 2 2 2 3 3 3 3 merization Irg2959 1 1 1 1 1 1 1 1 1 1 initiator Polyether- KP109 (50% sol.) (SiO content: 1 2 3 1 3.5 4.5 0.5 — — — modified 29% by mass, Mw 12,000) siloxane KP368 (SiO content: 90% by mass — — — — — — — 1 — — compound or more, Mw 7,000) KP306 (SiO content: 25% by mass, — — — — — — — — 1 — Mw 12,000) KP341 (SiO content: 15% by mass, — — — — — — — — — 1 Mw 11,000) Total (parts by mass) 100 100 100 100 100 100 100 100 100 100 Content of polyether-modified siloxane compound 3 6 9 4 12 15 1 6 6 6 with respect to total solid content (% by mass) Content ratio of polymerizable compound with 20 10 6.7 16 4.6 3.6 40 10 10 10 respect to parts by mass of polyether-modified siloxane compound 1 (parts by mass) Base Abrasion resistance 5 5 3 5 3 3 4 5 5 3 material: Bendability 5 5 5 5 5 5 5 5 5 5 ARES YP606 Chemical resistance 5 5 4 5 4 3 3 5 5 3 Adhesiveness 5 5 4 5 4 3 3 5 4 4 Ink jet jetting stability 5 5 4 5 3 3 4 3 5 5

TABLE 7 Example 11 12 13 14 15 16 17 18 19 20 Printing pattern 2 2 2 2 2 2 2 2 2 2 Solvent 3-Methoxybutyl acetate 82  82  82  82  — — 82  82  82  82  TEGMBE — — — — 82  — — — — — DEGDEE — — — — — 82  — — — — Oligomer CN9001 (bifunctional, Mw 3,250) 5 5 5 5 5 5 5 — 8 2 SHIKO UV-7600B (hexafunctional, 5 5 5 5 5 5 — 5 2 8 Mw 1,400) SHIKO UV-7550B (trifunctional, — — — — — — 5 — — — Mw 2,400) SHIKO UV-3310B (bifunctional, — — — — — — — 5 — — Mw 5,000) Resin Vinnol H14/36 2 2 2 2 2 2 2 2 2 2 Polymer- UV12 1 1 1 1 1 1 1 1 1 1 ization inhibitor Photopoly- Irg819 3 3 3 3 3 3 3 3 3 3 merization Irg2959 1 1 1 1 1 1 1 1 1 1 initiator Polyether- KP109 (50% sol.) (SiO content: — — — — 1 1 1 1 1 1 modified 29% by mass, Mw 12,000) siloxane KF-96H-10,000 CS (SiO content: 1 — — — — — — — — — compound 20% by mass or more, Mw 70,000) KF-96H-30,000 CS (SiO content: — 1 — — — — — — — — 20% by mass or more, Mw 90,000) KF-96H-100,000 CS (SiO content: — — 1 — — — — — — — 20% by mass or more, Mw 100,000) BYK-UV 3500 (SiO content: — — — 1 — — — — — — 30% by mass or more, Mw 3,500) Total (parts by mass) 100  100  100  100  100  100  100  100  100  100  Content of polyether-modified siloxane compound 6 6 6 6 3 3 3 3 3 3 with respect to total solid content (% by mass) Content ratio of polymerizable compound with 10  10  10  10  20  20  20  20  20  20  respect to parts by mass of polyether-modified siloxane compound 1 (parts by mass) Base Abrasion resistance 4 4 3 5 5 5 5 5 4 5 material: Bendability 5 5 5 4 5 5 5 5 5 3 ARES YP606 Chemical resistance 4 4 5 5 5 5 5 5 4 4 Adhesiveness 4 4 5 3 5 5 5 5 5 5 Ink jet jetting stability 4 3 3 5 5 5 5 3 5 5

TABLE 8 Example 21 22 23 24 25 26 27 28 29 Printing pattern 2 2 2 2 2 1 1 1 1 Solvent 3-Methoxybutyl acetate 82  84  78 57 44 71 66 67 69 Oligomer CN9001 (bifunctional, Mw 3,250) 5 5 2 10 10 12 12 12 12 SHIKO UV-7600B (hexafunctional, Mw 1,400) 5 5 2 10 10 3 3 3 3 Monomer PEA — — 10 15 28 — — — — Resin Vinnol H14/36 — — 2 2 2 2 2 2 2 Vinnol H11/59 2 — — — — — — — — Polymer- UV12 1 1 1 1 1 1 1 1 1 ization inhibitor Photopoly- Irg819 3 3 3 3 3 3 3 3 3 merization Irg2959 1 1 1 1 1 1 1 1 1 initiator Mill base Cyan — — — — — 6 — — — Magenta — — — — — — 11 — — Yellow — — — — — — — 10 — Black — — — — — — — — 8 Polyether- KP109 (50% sol.) (SiO content: 29% by mass, 1 1 1 1 1 1 1 1 1 modified Mw 12,000) siloxane compound Total (parts by mass) 100  100  100 100 100 100 100 100 100 Content of polyether-modified siloxane compound with 3 3 2 1 1 2 2 2 2 respect to total solid content (% by mass) Content ratio of polymerizable compound with respect to 20  20  28 70 96 30 30 30 30 parts by mass of polyether-modified siloxane compound 1 (parts by mass) Base Abrasion resistance 5 5 4 4 4 5 5 5 5 material: Bendability 5 5 5 5 5 5 5 5 5 ARES YP606 Chemical resistance 5 4 3 4 3 4 5 5 4 Adhesiveness 5 4 3 3 3 5 5 5 5 Ink jet jetting stability 3 5 5 5 5 4 4 4 4

TABLE 9 Comparative Example 1 2 3 4 5 6 Printing pattern 2 2 2 2 2 2 Solvent 3-Methoxybutyl acetate 81  80  80  81  81  35  Oligomer CN9001 (bifunctional, 5 5 5 5 5 8 Mw 3,250) SHIKO UV-7600B 5 5 5 5 5 7 (hexafunctional, Mw 1,400) Monomer PEA — — — — — 40  Resin Vinnol H14/36 2 2 2 2 2 2 Vinnol H11/59 2 2 2 2 2 2 Polymer- UV12 1 1 1 1 1 1 ization inhibitor Photopoly- Irg819 3 3 3 3 3 3 merization Irg2959 1 1 1 1 1 1 initiator Mill base Cyan — — — — — — Magenta — — — — — — Yellow — — — — — — Black — — — — — — Polyether- KP109 (50% sol.) (SiO content: — — — — — 1 modified 29% by mass, Mw 12,000) siloxane BYK 331 (SiO content: 10% by — 1 — — — — compound mass, Mw 2,500) Efka SL 3210 (SiO content: 9% — — 1 — — — by mass, Mw 1,500) Polyether- KP105 (30% sol.) — — — 3.3   — — modified siloxane compound Fluorine-based MEGAFACE RS-72-K — — — — 2.5   — surfactant (40% sol.) Total (parts by mass) 100  100  100  100  100  100  Content of polyether-modified siloxane 0 5 5 0 0 2 compound with respect to total solid content (% by mass) Content ratio of polymerizable compound — 10  10  — — 110  with respect to parts by mass of polyether- modified siloxane compound 1 (parts by mass) Base Abrasion resistance 1 2 1 1 2 3 material: Bendability 5 5 5 5 2 2 ARES YP606 Chemical resistance 2 2 2 2 2 2 Adhesiveness 5 3 3 3 3 3 Ink jet jetting stability 5 5 5 5 3 3 Comparative Example 7 8 9 10 11 Printing pattern 2 1 1 1 1 Solvent 3-Methoxybutyl acetate — 72  67  68  70  Oligomer CN9001 (bifunctional, 8 12  12  12  12  Mw 3,250) SHIKO UV-7600B 7 3 3 3 3 (hexafunctional, Mw 1,400) Monomer PEA 60  — — — — Resin Vinnol H14/36 2 2 2 2 2 Vinnol H11/59 2 — — — — Polymer- UV12 1 1 1 1 1 ization inhibitor Photopoly- Irg819 3 3 3 3 3 merization Irg2959 1 1 1 1 1 initiator Mill base Cyan — 6 — — — Magenta — — 11  — — Yellow — — — 10  — Black — — — — 8 Polyether- KP109 (50% sol.) (SiO content: 1 — — — — modified 29% by mass, Mw 12,000) siloxane BYK 331 (SiO content: 10% by — — — — — compound mass, Mw 2,500) Efka SL 3210 (SiO content: 9% — — — — — by mass, Mw 1,500) Polyether- KP105 (30% sol.) — — — — — modified siloxane compound Fluorine-based MEGAFACE RS-72-K — — — — — surfactant (40% sol.) Total (parts by mass) 85  100  100  100  100  Content of polyether-modified siloxane 1 0 0 0   0.04 compound with respect to total solid content (% by mass) Content ratio of polymerizable compound 150  — — — — with respect to parts by mass of polyether- modified siloxane compound 1 (parts by mass) Base Abrasion resistance 2 2 2 2 2 material: Bendability 2 5 5 5 5 ARES YP606 Chemical resistance 2 3 2 2 3 Adhesiveness 3 5 5 5 5 Ink jet jetting stability 3 4 4 4 4

The “SiO content” in Tables 6 to 9 represents the content of the siloxane structure in the compound.

As clearly seen from the results in Tables 6 to 9, it is found that in a case of using the ink jet liquid composition according to the embodiment of the present disclosure, and even in a case of using a base material having a concave-convex shape as a base material, the abrasion resistance, bendability, chemical resistance, and adhesiveness of the obtained cured film are excellent.

In addition, as clearly seen from the results in Tables 6 to 9, the ink jet liquid composition according to the embodiment of the present disclosure has excellent ink jet jetting stability.

In addition, as shown in Examples 1 to 7 in Table 6, in a case where the content of the polyether-modified siloxane compound is 2% by mass or more and 15% by mass or less with respect to the total solid content of the composition, the abrasion resistance, chemical resistance, and adhesiveness of the obtained cured film are further excellent, and the ink jet jettability is further excellent.

As shown in Examples 1 and 10 in Table 6, in a case where the content of the siloxane structure of the polyether-modified siloxane compound is 20% by mass or more with respect to the total mass of the polyether-modified siloxane compound, the abrasion resistance, chemical resistance, and adhesiveness of the obtained cured film are further excellent.

As shown in Example 1 in Table 6 and Example 14 in Table 7, in a case where the weight-average molecular weight of the polyether-modified siloxane compound is 5,000 or more, the bendability and adhesiveness of the obtained cured film are further excellent.

3. Printing of Pattern 2 after Changing Base Material

The abrasion resistance, bendability, chemical resistance, and adhesiveness of the prepared samples were evaluated based on the evaluation standards except that the liquid composition of Example 1, 8, or 9, or Comparative Example 1 or 2 shown in Table 10 was used on each base material shown in Table 10 as a transparent liquid composition by the ink jet printer.

The evaluation results are collectively shown in Table 10.

TABLE 10 Comparative Example Example 1 8 9 1 2 Base Abrasion 5 5 4 1 2 material: resistance CUPPUCCINO Bendability 5 5 5 5 5 CP-830 Chemical 5 5 4 2 2 resistance Adhesiveness 5 4 4 5 3 Base Abrasion 5 5 5 2 3 material: resistance MPI 1005 Bendability 5 5 5 5 5 Chemical 5 5 5 2 2 resistance Adhesiveness 5 5 4 5 4

In addition, the details of the base materials used in Examples are summarized shown in Table 11.

TABLE 11 Base material Supplier L2/L1 Gloss polyvinyl MPI 1005 Avery products 1.05 chloride sheet corporation Polyvinyl chloride CUPPUCCINO YAMAPLAS 1.21 (PVC) leather CP-830 CO., LTD. Polyvinyl chloride ARES YP606 YAMAPLAS 1.33 (PVC) leather CO., LTD.

As shown in Tables 6 and 10, it is found that in a case of using the ink jet liquid composition according to the embodiment of the present disclosure, for the various base materials having a concave-convex shape on the surface thereof, the abrasion resistance, bendability, chemical resistance, and adhesiveness of the obtained cured film are excellent.

Example 30

4. Pattern for Both Decorative Layer and Protective Layer Using Liquid Composition According to Embodiment of Present Disclosure

The used liquid composition was introduced into the ink jet printer and the pattern 2 was printed. As the coloring liquid composition, the liquid composition of Example 28 in Table 8 was used. A yellow solid image of a size of 20 cm×12 cm was printed and a base material having a decorative layer formed thereon was prepared. The liquid composition of Example 1 shown in Table 6 was used as a transparent liquid composition to form a protective layer on the decorative layer. The abrasion resistance, bendability, chemical resistance, and adhesiveness were evaluated for the prepared sample according to the above evaluation standards.

In the evaluation results, the abrasion resistance was 5, the bendability was 5, the chemical resistance was 5, and the adhesiveness was 5.

The entirety of the disclosure of Japanese Patent Application No. 2017-037215 filled on Feb. 28, 2017, is incorporated herein by reference.

All documents, patent applications and technical standards mentioned herein are incorporated in the present specification by reference to the same extent as if each individual document, patent application or technical standard was specifically and individually indicated to be incorporated by reference. 

What is claimed is:
 1. An ink jet liquid composition comprising: an organic solvent; a polymerizable compound; a photopolymerization initiator; and a polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, wherein a content of the organic solvent is 40% by mass or more and 90% by mass or less with respect to a total mass of the composition, and wherein a content of a siloxane structure of the polyether-modified siloxane compound is 20% by mass or more with respect to a total mass of the polyether-modified siloxane compound.
 2. The ink jet liquid composition according to claim 1, wherein the polyether-modified siloxane compound has a weight-average molecular weight of 5,000 or more and 100,000 or less.
 3. The ink jet liquid composition according to claim 1, wherein a content of the polyether-modified siloxane compound is 2% by mass or more and 15% by mass or less with respect to a total solid content of the composition.
 4. The ink jet liquid composition according to claim 1, wherein a mass ratio of the polyether-modified siloxane compound and the polymerizable compound is polyether-modified siloxane compound:polymerizable compound=1:5 to 1:30.
 5. The ink jet liquid composition according to claim 1, wherein the polymerizable compound includes a bifunctional urethane acrylate oligomer.
 6. The ink jet liquid composition according to claim 5, wherein the bifunctional urethane acrylate oligomer has a weight-average molecular weight of 3,000 or more and 20,000 or less.
 7. The ink jet liquid composition according to claim 1, wherein the ink jet liquid composition does not contain a colorant.
 8. The ink jet liquid composition according to claim 1 that is an ink jet liquid composition to be applied to a base material having a concave-convex shape in at least a part of a surface.
 9. An ink jet recording method comprising: a step of applying the ink jet liquid composition according to claim 1 to a base material by an ink jet recording head.
 10. The ink jet recording method according to claim 9, wherein the base material is a base material having a concave-convex shape in at least a part of a surface.
 11. An ink jet recording method comprising: a step of preparing a base material having a decorative layer formed thereon; a step of applying the ink jet liquid composition according to claim 8 to the decorative layer by an ink jet recording head; a step of drying the ink jet liquid composition on the decorative layer by applying heat; and a step of curing the ink jet liquid composition by irradiating the ink jet liquid composition with an ultraviolet ray, wherein the base material having the decorative layer formed thereon has a concave-convex shape in at least a part of a surface.
 12. An ink jet liquid composition comprising: an organic solvent; a polymerizable compound; a photopolymerization initiator; and a polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, wherein a content of the organic solvent is 40% by mass or more and 90% by mass or less with respect to a total mass of the composition, and wherein a content of the polyether-modified siloxane compound is 2% by mass or more and 15% by mass or less with respect to a total solid content of the composition.
 13. The ink jet liquid composition according to claim 12, wherein the polyether-modified siloxane compound has a weight-average molecular weight of 5,000 or more and 100,000 or less.
 14. The ink jet liquid composition according to claim 12, wherein a mass ratio of the polyether-modified siloxane compound and the polymerizable compound is polyether-modified siloxane compound:polymerizable compound=1:5 to 1:30.
 15. The ink jet liquid composition according to claim 12, wherein the polymerizable compound includes a bifunctional urethane acrylate oligomer.
 16. The ink jet liquid composition according to claim 15, wherein the bifunctional urethane acrylate oligomer has a weight-average molecular weight of 3,000 or more and 20,000 or less.
 17. An ink jet liquid composition comprising: an organic solvent; a polymerizable compound; a photopolymerization initiator; and a polyether-modified siloxane compound having a weight-average molecular weight of 3,000 or more, wherein a content of the organic solvent is 40% by mass or more and 90% by mass or less with respect to a total mass of the composition, and wherein a mass ratio of the polyether-modified siloxane compound and the polymerizable compound is polyether-modified siloxane compound:polymerizable compound=1:5 to 1:30.
 18. The ink jet liquid composition according to claim 17, wherein the polyether-modified siloxane compound has a weight-average molecular weight of 5,000 or more and 100,000 or less.
 19. The ink jet liquid composition according to claim 17, wherein the polymerizable compound includes a bifunctional urethane acrylate oligomer.
 20. The ink jet liquid composition according to claim 19, wherein the bifunctional urethane acrylate oligomer has a weight-average molecular weight of 3,000 or more and 20,000 or less. 